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Progressive pseudorheumatoid dysplasia

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PPD is an extremely rare disease. In the United States the disease is estimated to affect less than 5,000 people and approximately 1 per million people in the United Kingdom however it is believed to be more common in Turkey and the Middle East.
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Treatment for PPD is supportive. Anti-inflammatory drugs may be used for pain due to secondary osteoarthritis. More severe joint pain may be treated with surgery. Physical therapy, occupational therapy, may help with joint stiffness.
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gene, which encodes a signalling factor involved in cartilage homeostasis. Genomic changes to the gene result in a non-functional protein, which disrupts cartilage aintenance and bone growth. The disorder is inherited in an
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Bhavani, Gandham SriLakshmi; Shah, Hitesh; Shukla, Anju; Dalal, Ashwin; Girisha, Katta Mohan (1993), Adam, Margaret P.; Everman, David B.; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.),
17: 33:(PPD, PPRD), also known as progressive pseudorheumatoid arthropathy of childhood (PPAD), is a disorder of bone and cartilage that affects many joints. The disorder leads to 275:
Torreggiani, Sofia; Torcoletti, Marta; Campos-Xavier, Belinda; Baldo, Francesco; Agostoni, Carlo; Superti-Furga, Andrea; Filocamo, Giovanni (March 2019).
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Since symptoms of PPD are similar to juvenile rhematoid arthritis, people with PPD may be initially misdiagnosed.
252:"Progressive pseudorheumatoid dysplasia - About the Disease - Genetic and Rare Diseases Information Center" 394:
Chen, Wenji; Mo, Shiyan; Luo, Gui; Wang, Yanyan; Deng, Xiaohu; Zhu, Jian; Zhao, Wei (2018-09-10).
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and widening of the ends of the finger and toe bones as well as other tubular bones.
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Symptoms are present typically between ages three and six years.
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or through radiography with characteristic skeletal features.
336:"Progressive pseudorheumatoid dysplasia: MedlinePlus Genetics" 361: 370:, Seattle (WA): University of Washington, Seattle, 18:Spondyloepiphyseal dysplasia tarda progressive art 451: 80:Stiffness in the joints of the fingers and knees 51:Wnt1-inducible signalling protein 3 (WISP3) gene 228:NORD (National Organization for Rare Disorders) 393: 84:Symptoms that may develop over time include: 429: 411: 364:"Progressive Pseudorheumatoid Dysplasia" 224:"Progressive pseudorheumatoid dysplasia" 197:PPD has no severe effect on life span. 31:Progressive pseudorheumatoid disyplasia 14: 452: 357: 355: 330: 328: 326: 246: 244: 156: 112: 24: 25: 476: 352: 323: 241: 160: 116: 49:PPD is caused by changes in the 200: 91:enlarged finger and knee joints 387: 268: 216: 103:PPD is diagnosed by molecular 13: 1: 209: 192: 148: 98: 7: 65: 27:Bone and cartilage disorder 10: 481: 281:Rheumatology International 413:10.1186/s12969-018-0272-7 293:10.1007/s00296-018-4170-6 256:rarediseases.info.nih.gov 88:permanently bent fingers 74:Abnormal walking pattern 44: 400:Pediatric Rheumatology 53:, also known as the 60:autosomal recessive 172:. You can help by 128:. You can help by 190: 189: 146: 145: 16:(Redirected from 472: 444: 443: 433: 415: 391: 385: 384: 383: 382: 359: 350: 349: 347: 346: 332: 321: 320: 272: 266: 265: 263: 262: 248: 239: 238: 236: 235: 220: 185: 182: 164: 157: 141: 138: 120: 113: 77:Weakness/fatigue 21: 480: 479: 475: 474: 473: 471: 470: 469: 450: 449: 448: 447: 392: 388: 380: 378: 360: 353: 344: 342: 340:medlineplus.gov 334: 333: 324: 273: 269: 260: 258: 250: 249: 242: 233: 231: 222: 221: 217: 212: 203: 195: 186: 180: 177: 170:needs expansion 151: 142: 136: 133: 126:needs expansion 105:genetic testing 101: 68: 47: 28: 23: 22: 15: 12: 11: 5: 478: 468: 467: 462: 446: 445: 386: 351: 322: 287:(3): 441–452. 267: 240: 230:. 16 June 2022 214: 213: 211: 208: 202: 199: 194: 191: 188: 187: 181:September 2022 167: 165: 150: 147: 144: 143: 137:September 2022 123: 121: 100: 97: 96: 95: 92: 89: 82: 81: 78: 75: 67: 64: 46: 43: 26: 9: 6: 4: 3: 2: 477: 466: 463: 461: 460:Rare diseases 458: 457: 455: 441: 437: 432: 427: 423: 419: 414: 409: 405: 401: 397: 390: 377: 373: 369: 365: 358: 356: 341: 337: 331: 329: 327: 318: 314: 310: 306: 302: 298: 294: 290: 286: 282: 278: 271: 257: 253: 247: 245: 229: 225: 219: 215: 207: 198: 184: 175: 171: 168:This section 166: 163: 159: 158: 155: 140: 131: 127: 124:This section 122: 119: 115: 114: 111: 108: 106: 93: 90: 87: 86: 85: 79: 76: 73: 72: 71: 63: 61: 56: 52: 42: 40: 39:short stature 36: 32: 19: 465:Osteopathies 403: 399: 389: 379:, retrieved 368:GeneReviews® 367: 343:. Retrieved 339: 284: 280: 270: 259:. Retrieved 255: 232:. Retrieved 227: 218: 204: 201:Epidemiology 196: 178: 174:adding to it 169: 152: 134: 130:adding to it 125: 109: 102: 83: 69: 54: 48: 35:stiff joints 30: 29: 62:pattern. 454:Categories 381:2022-09-07 345:2022-09-07 261:2022-09-07 234:2022-09-07 210:References 422:1546-0096 406:(1): 55. 301:1437-160X 193:Prognosis 149:Treatment 99:Diagnosis 440:30200995 376:26610319 317:53528751 309:30327864 94:hip pain 66:Symptoms 431:6131911 438:  428:  420:  374:  315:  307:  299:  313:S2CID 45:Cause 436:PMID 418:ISSN 372:PMID 305:PMID 297:ISSN 55:CCN6 426:PMC 408:doi 289:doi 176:. 132:. 456:: 434:. 424:. 416:. 404:16 402:. 398:. 366:, 354:^ 338:. 325:^ 311:. 303:. 295:. 285:39 283:. 279:. 254:. 243:^ 226:. 37:, 442:. 410:: 348:. 319:. 291:: 264:. 237:. 183:) 179:( 139:) 135:( 20:)

Index

Spondyloepiphyseal dysplasia tarda progressive art
stiff joints
short stature
Wnt1-inducible signalling protein 3 (WISP3) gene
autosomal recessive
genetic testing

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"Progressive pseudorheumatoid dysplasia"


"Progressive pseudorheumatoid dysplasia - About the Disease - Genetic and Rare Diseases Information Center"
"Progressive pseudorheumatoid dysplasia: a rare childhood disease"
doi
10.1007/s00296-018-4170-6
ISSN
1437-160X
PMID
30327864
S2CID
53528751



"Progressive pseudorheumatoid dysplasia: MedlinePlus Genetics"


"Progressive Pseudorheumatoid Dysplasia"

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