Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia

Rare diseases are often misdiagnosed or receive a delayed diagnosis; thus, unfortunately, affected individuals may not receive optimal medical management. Here, we report a case of two siblings with a severe phenotype of progressive pseudorheumatoid dysplasia (PPD). Their onset of symptoms began at...

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Detalles Bibliográficos
Autores principales: Alawbathani, Salem, Kawalia, Amit, Karakaya, Mert, Altmüller, Janine, Nürnberg, Peter, Cirak, Sebahattin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793772/
https://www.ncbi.nlm.nih.gov/pubmed/29258992
http://dx.doi.org/10.1101/mcs.a002139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793772/
https://www.ncbi.nlm.nih.gov/pubmed/29258992
http://dx.doi.org/10.1101/mcs.a002139

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