78:
51:
1292:
Bardhan, Ajoy; Bruckner-Tuderman, Leena; Chapple, Iain L. C.; Fine, Jo-David; Harper, Natasha; Has, Cristina; Magin, Thomas M.; Marinkovich, M. Peter; Marshall, John F.; McGrath, John A.; Mellerio, Jemima E.; Polson, Rex; Heagerty, Adrian H. (2020-09-24). "Epidermolysis bullosa".
904:
Phornphutkul, Chanika; Introne, Wendy J.; Perry, Monique B.; Bernardini, Isa; Murphey, Mark D.; Fitzpatrick, Diana L.; Anderson, Paul D.; Huizing, Marjan; Anikster, Yair; Gerber, Lynn H.; Gahl, William A. (2002-12-26). "Natural
History of Alkaptonuria".
860:
Bernardini, Giulia; Braconi, Daniela; Zatkova, Andrea; Sireau, Nick; Kujawa, Mariusz J.; Introne, Wendy J.; Spiga, Ottavia; Geminiani, Michela; Gallagher, James A.; Ranganath, Lakshminarayan R.; Santucci, Annalisa (2024-03-07). "Alkaptonuria".
580:- unclassifiable systemic autoimmune disorders that do not meet any of the current classification requirements for connective tissue diseases yet have clinical and serological signs similar to connective tissue diseases.
1621:
Brito-Zerón, Pilar; Baldini, Chiara; Bootsma, Hendrika; Bowman, Simon J.; Jonsson, Roland; Mariette, Xavier; Sivils, Kathy; Theander, Elke; Tzioufas, Athanasios; Ramos-Casals, Manuel (2016-07-07). "Sjögren syndrome".
3205:
153:
affecting the primary structure of connective tissue, and (2) a variety of acquired diseases where the connective tissues are the site of multiple, more or less distinct immunological and inflammatory reactions.
3935:
2199:
216:. Many result in anomalies of the skeleton and joints, which can substantially impair normal growth and development. In contrast to acquired connective tissue diseases, these conditions are uncommon.
1849:
Tani, Chiara; Carli, Linda; Vagnani, Sabrina; Talarico, Rosaria; Baldini, Chiara; Mosca, Marta; Bombardieri, Stefano (2014). "The diagnosis and classification of mixed connective tissue disease".
4010:
3198:
2192:
3191:
2954:
2185:
1888:
Mosca, Marta; Tani, Chiara; Vagnani, Sabrina; Carli, Linda; Bombardieri, Stefano (2014). "The diagnosis and classification of undifferentiated connective tissue diseases".
1087:
Stattin, E.-L.; Tegner, Y.; Domellöf, M.; Dahl, N. (2008). "Familial osteochondritis dissecans associated with early osteoarthritis and disproportionate short stature".
142:
are all made of collagen. Skin and ligaments contain elastin. The proteins and the body's surrounding tissues may suffer damage when these connective tissues become
4158:
548:- uncommon multisystem autoimmune disease with an unclear etiology that is marked by progressive cartilaginous tissue loss and recurring episodes of inflammation.
4026:
3430:
514:- uncommon condition caused by protein mutations or changes in the body that result in twisted clusters of malformed proteins accumulating on organs and tissues.
1030:
Kaplan, Frederick S.; Le Merrer, Martine; Glaser, David L.; Pignolo, Robert J.; Goldsby, Robert E.; Kitterman, Joseph A.; Groppe, Jay; Shore, Eileen M. (2008).
255:- diverse collection of disorders distinguished by the fragility of soft connective tissues and widespread symptoms affecting the skin, ligaments, joints,
2681:
1426:
American
College of Rheumatology Subcommittee on Rheumatoid Arthritis Guidelines (2002). "Guidelines for the management of rheumatoid arthritis: 2002 Update".
3459:
3425:
2530:
192:; and (2) a number of acquired conditions where the connective tissues are the site of multiple, more or less distinct immune and inflammatory reactions.
2520:
390:- autosomal dominant condition linked to a wide range of systemic manifestations, such as skeletal, cutaneous, vascular, and craniofacial abnormalities.
2947:
2729:
1176:
Warady, Bradley A.; Agarwal, Rajiv; Bangalore, Sripal; Chapman, Arlene; Levin, Adeera; Stenvinkel, Peter; Toto, Robert D.; Chertow, Glenn M. (2020).
3366:
3866:
3361:
4273:
4168:
3862:
2940:
200:
Hereditary connective tissue disorders are a diverse set of broad, single-gene disorders that impact one or more of the main components of
1377:
Atwell, Karina; Michael, William; Dubey, Jared; James, Sarah; Martonffy, Andrea; Anderson, Scott; Rudin, Nathan; Schrager, Sarina (2021).
3674:
3454:
3449:
3439:
1990:
Spagnolo, Paolo; Cordier, Jean-François; Cottin, Vincent (2016-02-25). "Connective tissue diseases, multimorbidity and the ageing lung".
657:
4193:
3930:
3478:
577:
3813:
4153:
3748:
3473:
3405:
2293:
17:
4218:
3808:
3803:
2534:
2505:
2327:
2310:
3444:
3410:
2379:
2364:
3170:
2664:
359:
1510:
Fett, Nicole (2013). "Scleroderma: Nomenclature, etiology, pathogenesis, prognosis, and treatments: Facts and controversies".
3420:
3279:
2826:
844:
310:
3940:
3525:
2354:
1005:
3415:
3183:
2806:
2794:
1131:
523:
4233:
4178:
2908:
2801:
2739:
1553:
Mammen, Andrew L. (2010). "Dermatomyositis and polymyositis: Clinical presentation, autoantibodies, and pathogenesis".
554:- systemic autoimmune disease that shares characteristics with two or more other systemic autoimmune diseases, such as
409:
Acquired connective tissue diseases share certain clinical features, such as joint inflammation, inflammation of
3705:
3535:
3468:
3150:
2849:
2483:
741:
Kumar, Tarun; Sharma, Gurumayum Suraj; Singh, Laishram
Rajendrakumar (2016). "Homocystinuria: Therapeutic approach".
3818:
2987:
2789:
2657:
2298:
3722:
4243:
4223:
4173:
4143:
4020:
3793:
3498:
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3087:
2864:
2854:
2836:
2478:
551:
393:
3312:
1425:
3857:
3768:
3545:
3063:
2473:
2468:
2288:
4183:
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3763:
3686:
3400:
3346:
2992:
2821:
2691:
2676:
2493:
2369:
284:
176:
risks. Others may be due to environmental factors, or a combination of genetic and environmental influences.
3591:
3283:
2979:
2668:
2488:
2236:
567:
439:
417:, as well as a high frequency of involvement of various internal organs that are particularly rich in
349:
682:
Pepe, Guglielmina; Giusti, Betti; Sticchi, Elena; Abbate, Rosanna; Gensini, Gian; Nistri, Stefano (2016).
4208:
3925:
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2811:
2652:
2515:
2414:
2283:
2278:
2260:
280:
242:
3798:
3669:
3576:
3155:
2231:
2177:
1763:
Joly, Bérangère S.; Coppo, Paul; Veyradier, Agnès (2017-05-25). "Thrombotic thrombocytopenic purpura".
252:
4002:
3550:
3293:
2686:
2303:
2226:
505:
321:
162:
1469:
COJOCARU, Manole; COJOCARU, Inimioara
Mihaela; SILOSI, Isabela; VRABIE, Camelia Doina (2024-03-14).
77:
3843:
3831:
3789:
3775:
3753:
3743:
3739:
3647:
3642:
3637:
3633:
3625:
3596:
3029:
2859:
2248:
2243:
2105:
1709:
545:
387:
314:
290:
1597:
165:
can be (but are not necessarily) associated with collagen and blood vessel abnormalities that are
4121:
3540:
3503:
3351:
3038:
2816:
2604:
262:
2064:
4238:
4203:
4126:
3920:
3908:
3758:
3727:
3601:
3554:
3530:
3145:
3140:
2544:
2349:
633:
397:
3135:
2145:
157:
Diseases in which inflammation or weakness of collagen tends to occur are also referred to as
4103:
4014:
3390:
3239:
3007:
2719:
2500:
2432:
2359:
498:
and causes mucosal surfaces, especially those in the mouth and eyes, to become extremely dry.
377:
338:- autosomal dominant disorder distinguished by skeletal, ocular, and orofacial abnormalities.
300:
184:
Connective tissue diseases can be classified into two groups: (1) a group of relatively rare
2455:
520:- common articular cartilage degenerative disease linked to hypertrophic bone abnormalities.
106:. The body's structures are held together by connective tissues, consisting of two distinct
4093:
3995:
3513:
3130:
3058:
2882:
2744:
2696:
2525:
2510:
2389:
2339:
2322:
2273:
1336:
Gouda, Pishoy; Kay, Robert; Habib, Marina; Aziz, Amir; Aziza, Eitan; Welsh, Robert (2022).
555:
425:
3213:
2076:
1734:
784:
De Paepe, A; Malfait, F (2012). "The Ehlers–Danlos syndrome, a disorder with many faces".
8:
3901:
3780:
3330:
3288:
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3244:
3214:
3020:
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2734:
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2055:
583:
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491:
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2754:
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1963:
1928:
1523:
1487:
1470:
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1234:
1210:
1177:
1064:
1031:
982:
949:
836:
718:
683:
571:
443:
429:
304:
149:
The two main categories of connective tissue diseases are (1) a set of relatively rare
4188:
4148:
4070:
3945:
3889:
3823:
3488:
2724:
2610:
2557:
2427:
2409:
2399:
2015:
2007:
1968:
1950:
1909:
1901:
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1831:
1823:
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1639:
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1527:
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1408:
1400:
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1318:
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886:
878:
840:
809:
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797:
766:
758:
723:
705:
605:
418:
353:
335:
293:- rare multisystem disease marked by gradual calcification and fragmentation of
205:
201:
189:
103:
66:
59:
4075:
3710:
3521:
3493:
3102:
3083:
2898:
2779:
2749:
2562:
2394:
2036:
1999:
1958:
1945:
1940:
1893:
1854:
1815:
1772:
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1631:
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1435:
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1302:
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914:
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832:
793:
750:
713:
695:
600:
539:
531:
325:
185:
158:
150:
1338:"Clinical features and complications of Loeys-Dietz syndrome: A systematic review"
4098:
3616:
3165:
3025:
2997:
2110:
1776:
1395:
1378:
1354:
1337:
563:
527:
501:
471:
455:
410:
367:
341:
220:
3936:
Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
2003:
4213:
4198:
4131:
3913:
3884:
3734:
3698:
3652:
3611:
3307:
3230:
3068:
2384:
2318:
2040:
1897:
1858:
1819:
1193:
1100:
1047:
874:
538:
connected to diffuse microvascular platelet rich-thrombi, and microangiopathic
517:
495:
371:
363:
345:
234:
1678:
1379:"Diagnosis and Management of Hypermobility Spectrum Disorders in Primary Care"
1306:
754:
396:- a variety of connective tissue diseases that are marked by ongoing pain and
313:- rare and debilitating hereditary disorder characterized by progressive
4267:
4060:
3980:
3564:
2917:
2903:
2844:
2374:
2011:
1954:
1905:
1866:
1827:
1784:
1686:
1643:
1574:
1531:
1447:
1404:
1314:
1260:
1201:
1108:
1055:
973:
926:
882:
805:
762:
709:
294:
270:
223:- inherited as an autosomal dominant characteristic, due to mutations in the
965:
50:
4065:
4055:
3991:
3972:
3222:
3034:
2771:
2587:
2019:
1972:
1913:
1874:
1835:
1792:
1694:
1651:
1582:
1539:
1496:
1455:
1412:
1363:
1322:
1278:
1251:
1219:
1116:
1073:
991:
934:
890:
813:
770:
727:
559:
485:
475:
467:
459:
276:
266:
256:
246:
143:
139:
71:
1155:
4228:
3837:
3716:
3692:
3050:
2706:
2577:
2442:
2222:
2156:
2151:
2140:
1635:
918:
511:
449:
228:
3238:
2207:
2097:
2027:
Baildam, Eileen (2014). "Rare connective tissue diseases in childhood".
700:
3986:
3581:
3218:
2784:
2214:
481:
414:
381:
238:
166:
1439:
1226:
4248:
4011:
Template:Congenital malformations and deformations of skin appendages
3160:
2446:
2269:
2254:
2116:
1707:
1595:
1023:
827:
Marini, Joan C.; Cabral, Wayne A. (2018). "Osteogenesis
Imperfecta".
587:
433:
329:
131:
2165:
466:
that are clinically characterized by extramuscular symptoms, muscle
348:
is distinguished by structural abnormalities and malfunction in the
303:- a class of hereditary illnesses distinguished by the excretion of
3966:
3851:
3663:
3015:
1291:
535:
463:
446:
inflammatory disorder that can affect every organ in the body.
209:
173:
123:
115:
2121:
1080:
903:
384:
that are marked by blisters and mucocutaneous fragility.
2766:
2711:
213:
111:
107:
99:
3895:
3744:
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
2913:
2626:
2582:
2422:
2334:
1620:
504:- multisystem inflammatory illness that develops after group A
119:
1665:
Rullan, Eugenia; Sigal, Leonard H. (2001). "Rheumatic fever".
859:
4085:
1175:
1468:
1029:
2404:
432:
with an unclear cause that manifests as symmetric, erosive
224:
135:
127:
1710:"Amyloidosis: What It Is, Symptoms, Types & Treatment"
1235:"Congenital contractural arachnodactyly (Beals syndrome)"
1086:
404:
4159:
Congenital hypertrophy of the lateral fold of the hallux
2962:
1848:
1799:
494:- a systemic autoimmune illness that mostly affects the
452:- diverse collection of autoimmune fibrosing conditions.
195:
4027:
Template:DNA replication and repair-deficiency disorder
1376:
941:
681:
44:
Connective tissue disorder, collagen vascular diseases
1887:
1630:(1). Springer Science and Business Media LLC: 16047.
1285:
998:
2208:
Cutaneous keratosis, ulcer, atrophy, and necrobiosis
2087:
2065:"Connective Tissue Disease: Types, Symptoms, Causes"
1998:(5). European Respiratory Society (ERS): 1535–1558.
1708:
Cleveland Clinic medical professional (2022-07-05).
1596:
Cleveland Clinic medical professional (2024-05-01).
1383:
The
Journal of the American Board of Family Medicine
1329:
632:
Benedek, Thomas G.; Rodnan, Gerald P. (1998-07-24).
172:
Some connective tissue diseases have strong or weak
2521:
Palisaded neutrophilic and granulomatous dermatitis
586:- inflammatory musculoskeletal condition linked to
2682:Lupus erythematosus–lichen planus overlap syndrome
1808:Best Practice & Research Clinical Rheumatology
1762:
1301:(1). Springer Science and Business Media LLC: 78.
1036:Best Practice & Research Clinical Rheumatology
869:(1). Springer Science and Business Media LLC: 16.
3643:Diffuse nonepidermolytic palmoplantar keratoderma
1481:(4). Amaltea Medical, Editura Magister: 330–336.
1335:
1130:Bennett, James; McMurray, Scott (November 1990).
4265:
3367:Nonbullous congenital ichthyosiform erythroderma
1927:Ocampo D, Vanessa; Gladman, Dafna (2019-09-20).
1842:
1471:"Manifestations of Systemic Lupus Erythematosus"
740:
3832:Palmoplantar keratoderma and spastic paraplegia
1926:
1806:GERGELY, P (2004). "Relapsing polychondritis".
1658:
1232:
1178:"Alport Syndrome Classification and Management"
1129:
783:
380:- hereditary, diverse grouping of rare genetic
3638:Diffuse epidermolytic palmoplantar keratoderma
2730:Morphea–lichen sclerosus et atrophicus overlap
1726:
436:and, occasionally, extraarticular involvement.
4169:Congenital malformations of the dermatoglyphs
3199:
2948:
2193:
1598:"Vasculitis: Symptoms, Types & Treatment"
897:
853:
829:Genetics of Bone Biology and Skeletal Disease
734:
631:
269:, weakened bones, increased brittleness, and
826:
777:
627:
625:
623:
621:
526:- uncommon and potentially fatal thrombotic
2058:. National Library of Medicine. 2017-09-15.
1701:
1664:
1503:
650:
249:and its metabolites in the urine and blood.
4194:Melanotic neuroectodermal tumor of infancy
3931:Keratosis follicularis spinulosa decalvans
3362:Ichthyosis–sclerosing cholangitis syndrome
3206:
3192:
2955:
2941:
2200:
2186:
1589:
1555:Annals of the New York Academy of Sciences
1233:Tunçbilek, Ergül; Alanay, Yasemin (2006).
578:Undifferentiated connective tissue disease
366:, multiple flexion contractures, abnormal
76:
49:
4154:Congenital cartilaginous rest of the neck
3749:Focal palmoplantar and gingival keratosis
2294:Seborrheic keratosis with squamous atypia
1962:
1944:
1920:
1735:"Osteoarthritis: Diagnosis and Treatment"
1486:
1394:
1353:
1268:
1250:
1209:
1063:
981:
717:
699:
618:
362:- autosomal dominant disorder defined by
265:- hereditary condition marked by reduced
4219:Rapidly involuting congenital hemangioma
3809:Keratosis punctata of the palmar creases
3804:Keratosis punctata palmaris et plantaris
3675:Clouston's hidrotic ectodermal dysplasia
2535:Interstitial granulomatous drug reaction
2506:Annular elastolytic giant-cell granuloma
2328:Confluent and reticulated papillomatosis
2311:Keratosis punctata of the palmar creases
1123:
356:in other organs such as the eye and ear.
283:caused by mutations in the HGO gene and
2380:Multiple minute digitate hyperkeratosis
2365:Hyperkeratosis of the nipple and areola
1805:
1732:
1614:
1032:"Fibrodysplasia ossificans progressiva"
684:"Marfan syndrome: current perspectives"
245:deficit that causes a build-up of
14:
4266:
3171:Congenital contractural arachnodactyly
2237:Acrokeratosis paraneoplastica of Bazex
1552:
405:Autoimmune connective tissue disorders
360:Congenital contractural arachnodactyly
317:and congenital skeletal malformations.
3280:Congenital ichthyosiform erythroderma
3187:
2936:
2827:Atrophia maculosa varioliformis cutis
2531:Interstitial granulomatous dermatitis
2181:
1546:
1462:
947:
675:
311:Fibrodysplasia ossificans progressiva
196:Heritable connective tissue disorders
4274:Systemic connective tissue disorders
3941:Keratosis pilaris atrophicans faciei
3526:Dermatopathia pigmentosa reticularis
2355:Hyperkeratosis lenticularis perstans
1881:
1509:
1169:
688:The Application of Clinical Genetics
634:"Description, Types, & Symptoms"
2807:Acrodermatitis chronica atrophicans
1756:
1370:
1342:International Journal of Cardiology
820:
524:Thrombotic thrombocytopenic purpura
188:affecting the primary structure of
24:
4234:Superficial lymphatic malformation
4179:Congenital smooth muscle hamartoma
3648:Palmoplantar keratoderma of Sybert
3217:malformations and deformations of
2909:Poikiloderma vasculare atrophicans
2802:Atrophoderma of Pasini and Pierini
2740:Atrophoderma of Pasini and Pierini
1983:
1524:10.1016/j.clindermatol.2013.01.010
1419:
837:10.1016/b978-0-12-804182-6.00023-x
474:, and oftentimes the detection of
25:
4285:
3706:Scleroatrophic syndrome of Huriez
3536:Hypohidrotic ectodermal dysplasia
2850:Reactive perforating collagenosis
2484:Granuloma annulare in HIV disease
2048:
1239:Orphanet Journal of Rare Diseases
1136:Journal of Pediatric Orthopaedics
179:
3819:Porokeratosis plantaris discreta
3776:Striate palmoplantar keratoderma
2299:Reticulated seborrheic keratosis
2063:Dunkin, Mary Anne (2023-10-10).
1567:10.1111/j.1749-6632.2009.05119.x
1148:10.1097/01241398-199011000-00010
954:Archives of Disease in Childhood
798:10.1111/j.1399-0004.2012.01858.x
4244:Verrucous vascular malformation
4174:Congenital preauricular fistula
4144:Accessory nail of the fifth toe
4021:Template:Pigmentation disorders
3814:Schöpf–Schulz–Passarge syndrome
3794:Acrokeratoelastoidosis of Costa
3499:Laryngoonychocutaneous syndrome
3372:Ichthyosis linearis circumflexa
3357:Ichthyosis prematurity syndrome
3088:Mixed connective tissue disease
2865:Acquired perforating dermatosis
2855:Elastosis perforans serpiginosa
2795:Jadassohn–Pellizzari anetoderma
907:New England Journal of Medicine
552:Mixed connective tissue disease
394:Hypermobility spectrum disorder
3858:Erythrokeratodermia variabilis
3769:Pachyonychia congenita type II
3064:Progressive systemic sclerosis
2289:Irritated seborrheic keratosis
1946:10.12688/f1000research.19144.1
1624:Nature Reviews Disease Primers
1295:Nature Reviews Disease Primers
863:Nature Reviews Disease Primers
831:. Elsevier. pp. 397–420.
13:
1:
4184:Cystic lymphatic malformation
4137:Cavernous venous malformation
3764:Pachyonychia congenita type I
3687:Corneodermatoosseous syndrome
3347:Ichthyosis bullosa of Siemens
3151:Eosinophilia–myalgia syndrome
2822:Linear atrophoderma of Moulin
2494:Patch-type granuloma annulare
2370:Inverted follicular keratosis
2056:"Connective Tissue Disorders"
1892:. 48–49. Elsevier BV: 50–52.
1853:. 48–49. Elsevier BV: 46–49.
1733:Sinusas, Keith (2012-01-01).
1006:"Mucopolysaccharidoses (MPS)"
658:"Connective Tissue Disorders"
611:
285:homogentisate 1,2-dioxygenase
3592:Popliteal pterygium syndrome
3284:Epidermolytic hyperkeratosis
2980:Systemic lupus erythematosus
2790:Schweninger–Buzzi anetoderma
2489:Localized granuloma annulare
2077:"Connective tissue diseases"
2029:Paediatrics and Child Health
1992:European Respiratory Journal
1939:. F1000 Research Ltd: 1665.
1777:10.1182/blood-2016-10-709857
1667:Current Rheumatology Reports
1396:10.3122/jabfm.2021.04.200374
1355:10.1016/j.ijcard.2022.05.065
1089:Osteoarthritis and Cartilage
568:systemic lupus erythematosus
440:Systemic lupus erythematosus
350:glomerular basement membrane
332:from the surrounding tissue.
204:, such as ground substance (
7:
4224:Rosenthal–Kloepfer syndrome
4209:Omphalomesenteric duct cyst
3926:Keratolytic winter erythema
3586:Gerodermia osteodysplastica
2965:connective tissue disorders
2516:Necrobiotic xanthogranuloma
2415:Waxy keratosis of childhood
2284:Common seborrheic keratosis
2279:Clonal seborrheic keratosis
2261:Keratoderma blennorrhagicum
2004:10.1183/13993003.00829-2015
1814:(5). Elsevier BV: 723–738.
1518:(4). Elsevier BV: 432–437.
1188:(5). Elsevier BV: 639–649.
1095:(8). Elsevier BV: 890–896.
1042:(1). Elsevier BV: 191–205.
594:
241:metabolism brought on by a
10:
4290:
3799:Focal acral hyperkeratosis
3546:Ellis–van Creveld syndrome
2232:Paraneoplastic keratoderma
2041:10.1016/j.paed.2013.12.005
1898:10.1016/j.jaut.2014.01.019
1859:10.1016/j.jaut.2014.01.008
1820:10.1016/j.berh.2004.05.012
1428:Arthritis & Rheumatism
1194:10.1016/j.xkme.2020.05.014
1101:10.1016/j.joca.2007.11.009
1048:10.1016/j.berh.2007.11.007
950:"Pseudoxanthoma elasticum"
875:10.1038/s41572-024-00498-x
484:- disease that results in
374:, and muscular hypoplasia.
281:inborn error of metabolism
163:Collagen vascular diseases
96:collagen vascular diseases
92:connective tissue disorder
4114:
4084:
4048:
4039:
3958:
3877:
3723:Papillon–Lefèvre syndrome
3624:
3610:
3563:
3512:
3389:
3339:
3321:
3294:Harlequin-type ichthyosis
3270:
3252:
3229:
3123:
3100:
3079:
3049:
3006:
2993:Libman–Sacks endocarditis
2978:
2971:
2891:
2873:
2835:
2765:
2705:
2640:
2625:
2596:
2543:
2454:
2441:
2304:Dermatosis papulosa nigra
2227:Keratoderma climactericum
2213:
2131:
2091:
1739:American Family Physician
1679:10.1007/s11926-996-0016-4
1307:10.1038/s41572-020-0210-0
755:10.1016/j.cca.2016.04.002
506:streptococcal pharyngitis
322:osteochondritis dissecans
88:Connective tissue disease
65:
57:
48:
40:
36:Connective tissue disease
35:
18:Collagen vascular disease
3597:Pseudoxanthoma elasticum
3313:Sjögren–Larsson syndrome
3030:Juvenile dermatomyositis
2860:Perforating folliculitis
2812:Semicircular lipoatrophy
2249:Drug-induced keratoderma
546:Relapsing polychondritis
530:characterized by severe
315:heterotopic ossification
291:Pseudoxanthoma elasticum
243:cystathionine β-synthase
4122:Aplasia cutis congenita
3541:Focal dermal hypoplasia
3504:Skin fragility syndrome
3352:Ichthyosis follicularis
3039:Inclusion body myositis
2817:Follicular atrophoderma
2605:eosinophilic dermatosis
1890:Journal of Autoimmunity
1851:Journal of Autoimmunity
966:10.1136/adc.2004.062075
948:Laube, S (2005-07-01).
638:Encyclopedia Britannica
263:Osteogenesis imperfecta
4239:Thyroglossal duct cyst
4204:Nasolacrimal duct cyst
4127:Amniotic band syndrome
3921:Dyskeratosis congenita
3909:Dyskeratosis congenita
3759:Pachyonychia congenita
3670:Bart–Pumphrey syndrome
3602:Van der Woude syndrome
3577:Ehlers–Danlos syndrome
3156:Ehlers–Danlos syndrome
3146:Eosinophilic fasciitis
3141:Polymyalgia rheumatica
2545:Foreign body granuloma
2456:Necrobiotic/palisading
2350:Chronic scar keratosis
1512:Clinics in Dermatology
1252:10.1186/1750-1172-1-20
1010:Johns Hopkins Medicine
749:. Elsevier BV: 55–62.
259:, and internal organs.
253:Ehlers–Danlos syndrome
4104:Nevus flammeus nuchae
4015:Template:Phakomatoses
3987:Hereditary lymphedema
3551:Rapp–Hodgkin syndrome
3240:Congenital ichthyosis
3008:Inflammatory myopathy
2720:Localized scleroderma
2501:Necrobiosis lipoidica
2433:Cutis verticis gyrata
2360:Hydrocarbon keratosis
2244:Aquagenic keratoderma
1929:"Psoriatic arthritis"
411:serous membranes
378:Epidermolysis bullosa
301:Mucopolysaccharidosis
4094:Capillary hemangioma
3996:Urticaria pigmentosa
3754:Howel–Evans syndrome
3514:Ectodermal dysplasia
3455:Generalized atrophic
3131:IgG4-related disease
3059:Systemic scleroderma
2883:Pyoderma gangrenosum
2745:Pansclerotic morphea
2526:Rheumatoid nodulosis
2511:Granuloma multiforme
2390:Reactional keratosis
2340:Ichthyosis acquisita
2323:Acanthosis nigricans
2274:Seborrheic keratosis
2215:Epidermal thickening
1636:10.1038/nrdp.2016.47
919:10.1056/NEJMoa021736
743:Clinica Chimica Acta
556:rheumatoid arthritis
426:Rheumatoid arthritis
388:Loeys–Dietz syndrome
324:- separation of the
27:Category of diseases
3781:Tyrosinemia type II
3331:X-linked ichthyosis
3289:Lamellar ichthyosis
3262:Ichthyosis vulgaris
3245:erythrokeratodermia
3021:Dermatopolymyositis
2735:Generalized morphea
2573:Zirconium granuloma
2553:Beryllium granuloma
2421:other hypertrophy:
2375:Lichenoid keratosis
2345:Arsenical keratosis
1132:"Stickler Syndrome"
701:10.2147/TACG.S96233
584:Psoriatic arthritis
442:- chronic, complex
398:joint hypermobility
174:genetic inheritance
58:Different types of
4164:Congenital lip pit
3728:Haim–Munk syndrome
3680:Vohwinkel syndrome
3555:Hay–Wells syndrome
3531:Hay–Wells syndrome
3377:Ichthyosis hystrix
3303:Netherton syndrome
2755:Linear scleroderma
2568:Silicone granuloma
2464:Granuloma annulare
2132:External resources
572:systemic sclerosis
430:autoimmune disease
354:basement membranes
352:, as well as
305:mucopolysaccharide
227:gene that encodes
206:glycosaminoglycans
202:connective tissues
4261:
4260:
4257:
4256:
4189:Median raphe cyst
4149:Bronchogenic cyst
4071:PHACE association
4035:
4034:
3954:
3953:
3946:Keratosis pilaris
3890:Keratosis pilaris
3844:Carvajal syndrome
3824:Spiny keratoderma
3489:Costello syndrome
3385:
3384:
3181:
3180:
3096:
3095:
2930:
2929:
2926:
2925:
2725:Localized morphea
2697:Rowell's syndrome
2621:
2620:
2611:Granuloma faciale
2558:Mercury granuloma
2428:Hypertrophic scar
2410:Warty dyskeratoma
2400:Thermal keratosis
2175:
2174:
1771:(21): 2836–2846.
1440:10.1002/art.10148
913:(26): 2111–2121.
846:978-0-12-804182-6
786:Clinical Genetics
606:Connective tissue
419:connective tissue
336:Stickler syndrome
190:connective tissue
186:genetic disorders
159:collagen diseases
151:genetic disorders
104:connective tissue
85:
84:
60:connective tissue
30:Medical condition
16:(Redirected from
4281:
4076:Sinus pericranii
4046:
4045:
3902:Darier's disease
3711:Olmsted syndrome
3622:
3621:
3522:Naegeli syndrome
3494:Kindler syndrome
3250:
3249:
3236:
3235:
3208:
3201:
3194:
3185:
3184:
3136:Behçet's disease
3115:Sjögren syndrome
3103:hypersensitivity
3084:Overlap syndrome
2988:Drug-induced SLE
2976:
2975:
2957:
2950:
2943:
2934:
2933:
2899:Calcinosis cutis
2780:Lichen sclerosus
2750:Morphea profunda
2638:
2637:
2563:Silica granuloma
2452:
2451:
2395:Stucco keratosis
2202:
2195:
2188:
2179:
2178:
2089:
2088:
2084:
2072:
2059:
2044:
2023:
1977:
1976:
1966:
1948:
1924:
1918:
1917:
1885:
1879:
1878:
1846:
1840:
1839:
1803:
1797:
1796:
1760:
1754:
1753:
1751:
1750:
1730:
1724:
1723:
1721:
1720:
1714:Cleveland Clinic
1705:
1699:
1698:
1662:
1656:
1655:
1618:
1612:
1611:
1609:
1608:
1602:Cleveland Clinic
1593:
1587:
1586:
1550:
1544:
1543:
1507:
1501:
1500:
1490:
1466:
1460:
1459:
1423:
1417:
1416:
1398:
1374:
1368:
1367:
1357:
1333:
1327:
1326:
1289:
1283:
1282:
1272:
1254:
1230:
1224:
1223:
1213:
1173:
1167:
1166:
1164:
1162:
1127:
1121:
1120:
1084:
1078:
1077:
1067:
1027:
1021:
1020:
1018:
1017:
1002:
996:
995:
985:
945:
939:
938:
901:
895:
894:
857:
851:
850:
824:
818:
817:
781:
775:
774:
738:
732:
731:
721:
703:
679:
673:
672:
670:
669:
654:
648:
647:
645:
644:
629:
601:Overlap syndrome
540:hemolytic anemia
532:thrombocytopenia
492:Sjögren syndrome
472:muscle weakening
326:subchondral bone
102:that affect the
98:, refers to any
90:, also known as
81:
80:
53:
33:
32:
21:
4289:
4288:
4284:
4283:
4282:
4280:
4279:
4278:
4264:
4263:
4262:
4253:
4115:Other/ungrouped
4110:
4099:Port-wine stain
4080:
4041:
4031:
3950:
3873:
3615:
3606:
3559:
3508:
3393:
3381:
3335:
3317:
3266:
3243:
3225:
3212:
3182:
3177:
3166:Marfan syndrome
3119:
3092:
3075:
3045:
3026:Dermatomyositis
3002:
2998:Lupus nephritis
2967:
2961:
2931:
2922:
2887:
2869:
2831:
2770:
2761:
2710:
2701:
2643:
2642:Cutaneous lupus
2630:
2617:
2597:Other/ungrouped
2592:
2539:
2437:
2405:Viral keratosis
2209:
2206:
2176:
2171:
2170:
2127:
2126:
2100:
2075:
2062:
2054:
2051:
2026:
1989:
1986:
1984:Further reading
1981:
1980:
1925:
1921:
1886:
1882:
1847:
1843:
1804:
1800:
1761:
1757:
1748:
1746:
1731:
1727:
1718:
1716:
1706:
1702:
1663:
1659:
1619:
1615:
1606:
1604:
1594:
1590:
1551:
1547:
1508:
1504:
1467:
1463:
1424:
1420:
1375:
1371:
1334:
1330:
1290:
1286:
1231:
1227:
1182:Kidney Medicine
1174:
1170:
1160:
1158:
1128:
1124:
1085:
1081:
1028:
1024:
1015:
1013:
1004:
1003:
999:
946:
942:
902:
898:
858:
854:
847:
825:
821:
782:
778:
739:
735:
680:
676:
667:
665:
656:
655:
651:
642:
640:
630:
619:
614:
597:
564:dermatomyositis
528:microangiopathy
502:Rheumatic fever
496:exocrine glands
456:Dermatomyositis
407:
342:Alport syndrome
237:- condition of
221:Marfan syndrome
198:
182:
75:
31:
28:
23:
22:
15:
12:
11:
5:
4287:
4277:
4276:
4259:
4258:
4255:
4254:
4252:
4251:
4246:
4241:
4236:
4231:
4226:
4221:
4216:
4214:Poland anomaly
4211:
4206:
4201:
4199:Mongolian spot
4196:
4191:
4186:
4181:
4176:
4171:
4166:
4161:
4156:
4151:
4146:
4140:
4139:
4134:
4132:Branchial cyst
4129:
4124:
4118:
4116:
4112:
4111:
4109:
4108:
4107:
4106:
4096:
4090:
4088:
4082:
4081:
4079:
4078:
4073:
4068:
4063:
4058:
4052:
4050:
4043:
4037:
4036:
4033:
4032:
4006:
4005:
4000:
3999:
3998:
3989:
3977:
3976:
3975:
3962:
3960:
3956:
3955:
3952:
3951:
3949:
3948:
3943:
3938:
3933:
3928:
3923:
3917:
3916:
3914:Lelis syndrome
3911:
3906:
3905:
3904:
3892:
3887:
3885:Meleda disease
3881:
3879:
3875:
3874:
3872:
3871:
3870:
3869:
3860:
3848:
3847:
3846:
3834:
3827:
3826:
3821:
3816:
3811:
3806:
3801:
3796:
3786:
3785:
3784:
3783:
3778:
3773:
3772:
3771:
3766:
3756:
3751:
3746:
3737:
3735:Camisa disease
3732:
3731:
3730:
3725:
3713:
3708:
3703:
3702:
3701:
3699:Naxos syndrome
3689:
3684:
3683:
3682:
3677:
3672:
3656:
3655:
3653:Meleda disease
3650:
3645:
3640:
3630:
3628:
3619:
3612:Hyperkeratosis
3608:
3607:
3605:
3604:
3599:
3594:
3589:
3579:
3573:
3571:
3561:
3560:
3558:
3557:
3548:
3543:
3538:
3533:
3528:
3518:
3516:
3510:
3509:
3507:
3506:
3501:
3496:
3491:
3484:
3483:
3482:
3481:
3476:
3465:
3464:
3463:
3462:
3457:
3452:
3447:
3436:
3435:
3434:
3433:
3428:
3423:
3418:
3413:
3408:
3397:
3395:
3387:
3386:
3383:
3382:
3380:
3379:
3374:
3369:
3364:
3359:
3354:
3349:
3343:
3341:
3337:
3336:
3334:
3333:
3327:
3325:
3319:
3318:
3316:
3315:
3310:
3308:CHIME syndrome
3305:
3299:
3298:
3297:
3296:
3286:
3276:
3274:
3268:
3267:
3265:
3264:
3258:
3256:
3247:
3233:
3231:Genodermatosis
3227:
3226:
3211:
3210:
3203:
3196:
3188:
3179:
3178:
3176:
3175:
3174:
3173:
3168:
3158:
3153:
3148:
3143:
3138:
3133:
3127:
3125:
3121:
3120:
3118:
3117:
3111:
3109:
3098:
3097:
3094:
3093:
3091:
3090:
3080:
3077:
3076:
3074:
3073:
3072:
3071:
3069:CREST syndrome
3066:
3055:
3053:
3047:
3046:
3044:
3043:
3042:
3041:
3032:
3018:
3012:
3010:
3004:
3003:
3001:
3000:
2995:
2990:
2984:
2982:
2973:
2969:
2968:
2960:
2959:
2952:
2945:
2937:
2928:
2927:
2924:
2923:
2921:
2920:
2911:
2906:
2901:
2895:
2893:
2889:
2888:
2886:
2885:
2879:
2877:
2871:
2870:
2868:
2867:
2862:
2857:
2852:
2847:
2841:
2839:
2833:
2832:
2830:
2829:
2824:
2819:
2814:
2809:
2804:
2799:
2798:
2797:
2792:
2782:
2776:
2774:
2763:
2762:
2760:
2759:
2758:
2757:
2752:
2747:
2742:
2737:
2732:
2727:
2716:
2714:
2703:
2702:
2700:
2699:
2694:
2689:
2684:
2679:
2672:
2671:
2661:
2660:
2655:
2648:
2646:
2635:
2623:
2622:
2619:
2618:
2616:
2615:
2614:
2613:
2600:
2598:
2594:
2593:
2591:
2590:
2585:
2580:
2575:
2570:
2565:
2560:
2555:
2549:
2547:
2541:
2540:
2538:
2537:
2528:
2523:
2518:
2513:
2508:
2503:
2498:
2497:
2496:
2491:
2486:
2481:
2476:
2471:
2460:
2458:
2449:
2439:
2438:
2436:
2435:
2430:
2425:
2418:
2417:
2412:
2407:
2402:
2397:
2392:
2387:
2385:PUVA keratosis
2382:
2377:
2372:
2367:
2362:
2357:
2352:
2347:
2342:
2337:
2332:
2331:
2330:
2319:hyperkeratosis
2314:
2313:
2308:
2307:
2306:
2301:
2296:
2291:
2286:
2281:
2266:
2265:
2264:
2263:
2251:
2246:
2241:
2240:
2239:
2229:
2219:
2217:
2211:
2210:
2205:
2204:
2197:
2190:
2182:
2173:
2172:
2169:
2168:
2159:
2148:
2136:
2135:
2133:
2129:
2128:
2125:
2124:
2113:
2101:
2096:
2095:
2093:
2092:Classification
2086:
2085:
2073:
2060:
2050:
2049:External links
2047:
2046:
2045:
2024:
1985:
1982:
1979:
1978:
1919:
1880:
1841:
1798:
1755:
1725:
1700:
1673:(5): 445–452.
1657:
1613:
1588:
1561:(1): 134–153.
1545:
1502:
1461:
1434:(2): 328–346.
1418:
1389:(4): 838–848.
1369:
1328:
1284:
1225:
1168:
1142:(6): 760–763.
1122:
1079:
1022:
997:
960:(7): 754–756.
940:
896:
852:
845:
819:
776:
733:
674:
649:
616:
615:
613:
610:
609:
608:
603:
596:
593:
592:
591:
581:
575:
549:
543:
521:
518:Osteoarthritis
515:
509:
499:
489:
479:
476:autoantibodies
453:
447:
437:
406:
403:
402:
401:
391:
385:
375:
372:kyphoscoliosis
364:arachnodactyly
357:
346:kidney disease
339:
333:
318:
308:
298:
295:elastic fibres
288:
274:
260:
250:
235:Homocystinuria
232:
197:
194:
181:
180:Classification
178:
83:
82:
69:
63:
62:
55:
54:
46:
45:
42:
38:
37:
29:
26:
9:
6:
4:
3:
2:
4286:
4275:
4272:
4271:
4269:
4250:
4247:
4245:
4242:
4240:
4237:
4235:
4232:
4230:
4227:
4225:
4222:
4220:
4217:
4215:
4212:
4210:
4207:
4205:
4202:
4200:
4197:
4195:
4192:
4190:
4187:
4185:
4182:
4180:
4177:
4175:
4172:
4170:
4167:
4165:
4162:
4160:
4157:
4155:
4152:
4150:
4147:
4145:
4142:
4141:
4138:
4135:
4133:
4130:
4128:
4125:
4123:
4120:
4119:
4117:
4113:
4105:
4102:
4101:
4100:
4097:
4095:
4092:
4091:
4089:
4087:
4083:
4077:
4074:
4072:
4069:
4067:
4064:
4062:
4061:Encephalocele
4059:
4057:
4054:
4053:
4051:
4047:
4044:
4040:Developmental
4038:
4030:
4029:
4028:
4023:
4022:
4017:
4016:
4012:
4004:
4003:Hailey–Hailey
4001:
3997:
3993:
3990:
3988:
3985:
3984:
3983:
3982:
3981:immune system
3978:
3974:
3971:
3970:
3969:
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3964:
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3644:
3641:
3639:
3635:
3632:
3631:
3629:
3627:
3623:
3620:
3618:
3617:keratinopathy
3613:
3609:
3603:
3600:
3598:
3595:
3593:
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3587:
3583:
3580:
3578:
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3404:
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3392:
3388:
3378:
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3159:
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3112:
3110:
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3089:
3085:
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3070:
3067:
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2999:
2996:
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2989:
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2977:
2974:
2970:
2966:
2958:
2953:
2951:
2946:
2944:
2939:
2938:
2935:
2919:
2918:Pseudo-ainhum
2915:
2912:
2910:
2907:
2905:
2904:Sclerodactyly
2902:
2900:
2897:
2896:
2894:
2890:
2884:
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2880:
2878:
2876:
2872:
2866:
2863:
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2858:
2856:
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2851:
2848:
2846:
2845:Kyrle disease
2843:
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2818:
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2670:
2666:
2663:
2662:
2659:
2656:
2654:
2650:
2649:
2647:
2645:
2644:erythematosus
2639:
2636:
2634:
2628:
2624:
2612:
2609:
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2606:
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2167:
2163:
2160:
2158:
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2143:
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2138:
2137:
2134:
2130:
2123:
2119:
2118:
2114:
2112:
2108:
2107:
2103:
2102:
2099:
2094:
2090:
2083:. 2023-10-26.
2082:
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2061:
2057:
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2021:
2017:
2013:
2009:
2005:
2001:
1997:
1993:
1988:
1987:
1974:
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1965:
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1942:
1938:
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1933:F1000Research
1930:
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967:
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868:
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830:
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772:
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764:
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541:
537:
533:
529:
525:
522:
519:
516:
513:
510:
507:
503:
500:
497:
493:
490:
488:inflammation.
487:
483:
480:
477:
473:
469:
465:
462:- autoimmune
461:
457:
454:
451:
448:
445:
441:
438:
435:
431:
427:
424:
423:
422:
420:
416:
412:
399:
395:
392:
389:
386:
383:
379:
376:
373:
369:
365:
361:
358:
355:
351:
347:
344:- hereditary
343:
340:
337:
334:
331:
327:
323:
319:
316:
312:
309:
307:in the urine.
306:
302:
299:
296:
292:
289:
286:
282:
278:
275:
272:
271:short stature
268:
264:
261:
258:
257:blood vessels
254:
251:
248:
244:
240:
236:
233:
230:
226:
222:
219:
218:
217:
215:
211:
207:
203:
193:
191:
187:
177:
175:
170:
168:
164:
160:
155:
152:
147:
145:
141:
140:blood vessels
137:
133:
129:
125:
121:
117:
113:
109:
105:
101:
97:
93:
89:
79:
73:
70:
68:
64:
61:
56:
52:
47:
43:
39:
34:
19:
4066:Nasal glioma
4056:Dermoid cyst
4025:
4019:
4008:
4007:
3992:Mastocytosis
3979:
3973:EEM syndrome
3965:
3894:
3850:
3836:
3715:
3691:
3662:
3568:
3223:skin disease
3035:Polymyositis
2964:
2772:atrophoderma
2658:Panniculitis
2632:
2603:
2588:Carbon stain
2479:Subcutaneous
2253:
2161:
2150:
2139:
2115:
2104:
2080:
2068:
2035:(2): 51–57.
2032:
2028:
1995:
1991:
1936:
1932:
1922:
1889:
1883:
1850:
1844:
1811:
1807:
1801:
1768:
1764:
1758:
1747:. Retrieved
1742:
1738:
1728:
1717:. Retrieved
1713:
1703:
1670:
1666:
1660:
1627:
1623:
1616:
1605:. Retrieved
1601:
1591:
1558:
1554:
1548:
1515:
1511:
1505:
1478:
1474:
1464:
1431:
1427:
1421:
1386:
1382:
1372:
1345:
1341:
1331:
1298:
1294:
1287:
1242:
1238:
1228:
1185:
1181:
1171:
1159:. Retrieved
1139:
1135:
1125:
1092:
1088:
1082:
1039:
1035:
1025:
1014:. Retrieved
1012:. 2021-08-08
1009:
1000:
957:
953:
943:
910:
906:
899:
866:
862:
855:
828:
822:
789:
785:
779:
746:
742:
736:
691:
687:
677:
666:. Retrieved
664:. 2020-06-08
662:Cedars-Sinai
661:
652:
641:. Retrieved
637:
560:polymyositis
486:blood vessel
468:inflammation
460:polymyositis
408:
277:Alkaptonuria
247:homocysteine
199:
183:
171:
156:
148:
95:
91:
87:
86:
72:Rheumatology
4229:Skin dimple
3838:desmoplakin
3830:ungrouped:
3717:Cathepsin C
3693:plakoglobin
3394:and related
3051:Scleroderma
2837:Perforating
2707:Scleroderma
2675:ungrouped:
2578:Soot tattoo
2474:Generalized
2469:Perforating
2443:Necrobiosis
2223:keratoderma
2152:Radiopaedia
2141:MedlinePlus
1475:Mædica
1348:: 158–167.
792:(1): 1–11.
512:Amyloidosis
470:, proximal
450:Scleroderma
287:deficiency.
229:fibrillin 1
169:in nature.
41:Other names
3659:syndromic
3582:Cutis laxa
3569:Connective
3219:integument
3215:Congenital
3107:autoimmune
2875:Skin ulcer
2785:Anetoderma
2651:chronic:
2631:localized
1749:2024-07-16
1745:(1): 49–56
1719:2024-07-16
1607:2024-07-15
1016:2024-07-15
668:2024-07-16
643:2024-07-15
612:References
482:Vasculitis
464:myopathies
444:autoimmune
415:vasculitis
382:dermatoses
239:methionine
167:autoimmune
4249:Birthmark
4042:anomalies
4009:see also
3487:related:
3340:Ungrouped
3161:fibrillin
2963:Systemic
2692:Verrucous
2677:Chilblain
2447:granuloma
2270:keratosis
2255:psoriasis
2122:105969002
2117:SNOMED CT
2012:0903-1936
1955:2046-1402
1906:0896-8411
1867:0896-8411
1828:1521-6942
1785:0006-4971
1687:1523-3774
1644:2056-676X
1575:0077-8923
1532:0738-081X
1448:0004-3591
1405:1557-2625
1315:2056-676X
1261:1750-1172
1245:(1): 20.
1202:2590-0595
1109:1063-4584
1056:1521-6942
974:0003-9888
927:0028-4793
883:2056-676X
806:0009-9163
763:0009-8981
710:1178-704X
694:: 55–65.
588:psoriasis
434:synovitis
370:, severe
330:cartilage
320:Familial
267:bone mass
132:cartilage
124:ligaments
67:Specialty
4268:Category
3967:cadherin
3852:connexin
3790:punctate
3664:connexin
3016:Myositis
2767:Atrophic
2669:Neonatal
2665:subacute
2166:Q1779300
2081:DermNet®
2020:26917611
1973:31583079
1914:24518855
1875:24461387
1836:15454129
1793:28416507
1695:11564377
1652:27383445
1583:20146695
1540:23806160
1497:22879850
1456:11840435
1413:34312277
1364:35662564
1323:32973163
1279:16740166
1220:33094278
1117:18226555
1074:18328989
992:15970621
935:12501223
891:38453957
814:22353005
771:27059523
728:27274304
595:See also
536:ischemia
534:, organ
210:collagen
144:inflamed
116:collagen
108:proteins
100:disorder
4049:Midline
3634:diffuse
3565:Elastic
2972:General
2712:Morphea
2653:Discoid
2162:Scholia
2111:D003240
1964:6758836
1488:3391953
1270:1524931
1211:7568086
1161:15 July
1156:2250061
1065:2424023
983:1720489
719:4869846
214:elastin
120:Tendons
112:elastin
3896:ATP2A2
3460:JEB-PA
3431:EBS-MP
3426:EBS-MD
3421:EBS-OG
3416:EBS-DM
3411:EBS-WC
3101:Other
2914:Ainhum
2627:Dermis
2583:Tattoo
2423:Keloid
2335:Callus
2317:other
2146:001223
2018:
2010:
1971:
1961:
1953:
1912:
1904:
1873:
1865:
1834:
1826:
1791:
1783:
1693:
1685:
1650:
1642:
1581:
1573:
1538:
1530:
1495:
1485:
1454:
1446:
1411:
1403:
1362:
1321:
1313:
1277:
1267:
1259:
1218:
1208:
1200:
1154:
1115:
1107:
1072:
1062:
1054:
990:
980:
972:
933:
925:
889:
881:
843:
812:
804:
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