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List of fibrinogen disorders

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43:, a form of congenital hypofibrinogenemia in which specific hereditary mutations in fibrinogen cause it to accumulate in, and damage, liver cells. The disorder may lead to abnormal bleeding and thrombosis but also to 73:(i.e. wrong amount of sugar residues) added to an otherwise normal fibrinogen. The incorrectly glycosalated fibrinogen is dysfunctional and may cause pathological episodes of bleeding and/or blood clotting. 69:, a disorder in which normal levels of fibrinogen are composed at least in part of a dysfunctional fibrinogen due to an acquired disorder (e.g. liver disease) that leads to the synthesis of an incorrectly 172:
Casini A, Sokollik C, Lukowski SW, Lurz E, Rieubland C, de Moerloose P, Neerman-Arbez M (2015). "Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature".
53:, an inherited disorder in which normal levels of fibrinogen composed at least in part of a dysfunctional fibrinogen may cause abnormal bleeding and thrombosis. 37:, an inherited disorder in which blood may not clot normally due to reduced levels of fibrinogen; the disorder may cause abnormal bleeding and thrombosis. 31:, an inherited blood disorder in which blood does not clot normally due to the lack of fibrinogen; the disorder causes abnormal bleeding and thrombosis. 215:
Casini A, Neerman-Arbez M, Ariëns RA, de Moerloose P (2015). "Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management".
360:"Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation" 59:, a form of dysfibrinogenemia in which certain fibrinogen mutations cause blood fibrinogen to accumulate in the kidney and cause one type of 89:, an acquired disorder in which fibrinogen precipitates at cold temperatures and may lead to the intravascular precipitation of fibrinogen, 83:
levels of fibrinogen composed at least in part of a dysfunctional fibrinogen may cause pathological episodes of bleeding or blood clotting.
40: 56: 129:
Casini A, de Moerloose P, Neerman-Arbez M (2016). "Clinical Features and Management of Congenital Fibrinogen Deficiencies".
16:
Fibrinogen disorders are a set of hereditary or acquired abnormalities in the quantity and/or quality of circulating
66: 258:
Gillmore JD, Lachmann HJ, Rowczenio D, Gilbertson JA, Zeng CH, Liu ZH, Li LS, Wechalekar A, Hawkins PN (2009).
34: 24:
or the deposition of fibrinogen in the liver, kidneys, or other organs and tissues. These disorders include:
456: 60: 28: 260:"Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosis" 400: 76: 107: 8: 358:
Casini A, Brungs T, Lavenu-Bombled C, Vilar R, Neerman-Arbez M, de Moerloose P (2017).
335: 308: 284: 259: 240: 197: 154: 86: 433: 381: 340: 289: 232: 189: 146: 50: 244: 201: 158: 423: 415: 371: 330: 320: 279: 271: 224: 181: 138: 401:"Clinical conditions responsible for hyperviscosity and skin ulcers complications" 21: 450: 70: 437: 385: 344: 293: 275: 236: 193: 150: 142: 428: 325: 94: 17: 419: 376: 359: 228: 185: 63:; the disorder is not associated with abnormal bleeding or thrombosis. 214: 44: 257: 357: 128: 90: 171: 20:. The disorders may lead to pathological bleeding and/or 399:
Caimi G, Canino B, Lo Presti R, Urso C, Hopps E (2017).
398: 93:, and other circulating proteins thereby causing the 309:"Acquired hypofibrinogenemia: current perspectives" 448: 306: 124: 122: 264:Journal of the American Society of Nephrology 392: 351: 300: 251: 208: 165: 119: 408:Clinical Hemorheology and Microcirculation 97:of various tissues and bodily extremities. 57:Hereditary fibrinogen Aα-Chain amyloidosis 427: 375: 334: 324: 283: 449: 364:Journal of Thrombosis and Haemostasis 217:Journal of Thrombosis and Haemostasis 131:Seminars in Thrombosis and Hemostasis 13: 14: 468: 79:, an inherited disorder in which 307:Besser MW, MacDonald SG (2016). 77:Congenital hypodysfibrinogenemia 108:Fibrinogen#Fibrinogen disorders 1: 113: 35:Congenital hypofibrinogenemia 51:Congenital dysfibrinogenemia 7: 101: 10: 473: 67:Acquired dysfibrinogenemia 61:familial renal amyloidosis 41:Fibrinogen storage disease 29:Congenital afibrinogenemia 313:Journal of Blood Medicine 276:10.1681/ASN.2008060614 143:10.1055/s-0036-1571339 326:10.2147/JBM.S90693 87:Cryofibrinogenemia 457:Lists of diseases 420:10.3233/CH-160218 377:10.1111/jth.13655 229:10.1111/jth.12916 186:10.1111/hae.12719 464: 442: 441: 431: 405: 396: 390: 389: 379: 355: 349: 348: 338: 328: 304: 298: 297: 287: 255: 249: 248: 212: 206: 205: 169: 163: 162: 126: 472: 471: 467: 466: 465: 463: 462: 461: 447: 446: 445: 403: 397: 393: 356: 352: 305: 301: 256: 252: 213: 209: 170: 166: 127: 120: 116: 104: 12: 11: 5: 470: 460: 459: 444: 443: 391: 370:(5): 876–888. 350: 299: 250: 207: 164: 117: 115: 112: 111: 110: 103: 100: 99: 98: 84: 74: 64: 54: 48: 38: 32: 22:blood clotting 9: 6: 4: 3: 2: 469: 458: 455: 454: 452: 439: 435: 430: 425: 421: 417: 413: 409: 402: 395: 387: 383: 378: 373: 369: 365: 361: 354: 346: 342: 337: 332: 327: 322: 318: 314: 310: 303: 295: 291: 286: 281: 277: 273: 270:(2): 444–51. 269: 265: 261: 254: 246: 242: 238: 234: 230: 226: 223:(6): 909–19. 222: 218: 211: 203: 199: 195: 191: 187: 183: 179: 175: 168: 160: 156: 152: 148: 144: 140: 137:(4): 366–74. 136: 132: 125: 123: 118: 109: 106: 105: 96: 92: 88: 85: 82: 78: 75: 72: 68: 65: 62: 58: 55: 52: 49: 46: 42: 39: 36: 33: 30: 27: 26: 25: 23: 19: 429:10447/238851 414:(1): 25–34. 411: 407: 394: 367: 363: 353: 316: 312: 302: 267: 263: 253: 220: 216: 210: 180:(6): 820–7. 177: 173: 167: 134: 130: 80: 71:glycosylated 15: 319:: 217–225. 174:Haemophilia 18:fibrinogens 114:References 95:infarction 45:cirrhosis 451:Category 438:28550239 386:28211264 345:27713652 294:19073821 245:10955092 237:25816717 202:44911581 194:25990487 159:12038872 151:27019462 102:See also 336:5045218 285:2637055 436:  384:  343:  333:  292:  282:  243:  235:  200:  192:  157:  149:  91:fibrin 404:(PDF) 241:S2CID 198:S2CID 155:S2CID 434:PMID 382:PMID 341:PMID 290:PMID 233:PMID 190:PMID 147:PMID 424:hdl 416:doi 372:doi 331:PMC 321:doi 280:PMC 272:doi 225:doi 182:doi 139:doi 81:low 453:: 432:. 422:. 412:67 410:. 406:. 380:. 368:15 366:. 362:. 339:. 329:. 315:. 311:. 288:. 278:. 268:20 266:. 262:. 239:. 231:. 221:13 219:. 196:. 188:. 178:21 176:. 153:. 145:. 135:42 133:. 121:^ 440:. 426:: 418:: 388:. 374:: 347:. 323:: 317:7 296:. 274:: 247:. 227:: 204:. 184:: 161:. 141:: 47:.

Index

fibrinogens
blood clotting
Congenital afibrinogenemia
Congenital hypofibrinogenemia
Fibrinogen storage disease
cirrhosis
Congenital dysfibrinogenemia
Hereditary fibrinogen Aα-Chain amyloidosis
familial renal amyloidosis
Acquired dysfibrinogenemia
glycosylated
Congenital hypodysfibrinogenemia
Cryofibrinogenemia
fibrin
infarction
Fibrinogen#Fibrinogen disorders


doi
10.1055/s-0036-1571339
PMID
27019462
S2CID
12038872
doi
10.1111/hae.12719
PMID
25990487
S2CID
44911581

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