Progressive pseudorheumatoid dysplasia involving a novel WISP3 mutation and sacroiliac and hip arthritis: A case report and literature review

Progressive pseudorheumatoid dysplasia (PPRD) is a rare autosomal recessive genetic disease caused by mutations in the Wnt1-inducible signaling pathway protein 3 gene. PPRD is considered a noninflammatory disease, and involvement of the sacroiliac joint and hip arthritis have not been reported previ...

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Detalles Bibliográficos
Autores principales: Wang, Weitao, Xiao, Guangzhi, Han, Qing, Ding, Jin, Xie, Ronghua, Jia, Junfeng, Leng, Nan, Zheng, Zhaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
3600
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328645/
https://www.ncbi.nlm.nih.gov/pubmed/37417608
http://dx.doi.org/10.1097/MD.0000000000034099

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328645/
https://www.ncbi.nlm.nih.gov/pubmed/37417608
http://dx.doi.org/10.1097/MD.0000000000034099

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