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Arthritis und Rheuma 2013; 33(01): 34-36
DOI: 10.1055/s-0037-1618159
DOI: 10.1055/s-0037-1618159
Kinderrheumatologie: Kasuistik
Seltene Differenzialdiagnose der therapierefraktären juvenilen seronegativen Polyarthritis
Ein FallberichtFurther Information
Publication History
Publication Date:
27 December 2017 (online)

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Literatur
- 1 Wynne-Davies R, Hall C, Ansell BM. Spondyloepiphysial dysplasia tarda with progressive arthropathy. A “new” disorder of autosomal recessive inheritance. J Bone Joint Surg Br 1982; 64: 442-445.
- 2 Spranger J, Albert C, Schilling F. et al. Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritis. Eur J Pediatr 1983; 140: 34-40.
- 3 Hurvitz JR, Suwairi WM, Van Hul W. et al. Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia. Nat Genet 1999; 23: 94-98.
- 4 Garcia Segarra N, Mittaz L, Campos-Xavier AB. et al. The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): A review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals. Am J Med Genet Part C Semin Med Genet 2012; 160 C: 217-229.