Osteoarticular Manifestations of Prolidase Deficiency and Disability: Case Reports of Two Moroccan Sisters

Prolidase deficiency (PD) is a rare autosomal recessive disorder that has symptoms such as chronic skin ulcers, dysmorphic facies, cognitive retardation, hematological anomalies, splenomegaly, and chronic infections. Bone and joint abnormalities were referred occasionally and included the signs and...

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Detalles Bibliográficos
Autores principales: Asly, Mouna, Eljazouly, Madiha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502436/
https://www.ncbi.nlm.nih.gov/pubmed/34660074
http://dx.doi.org/10.7759/cureus.17875

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502436/
https://www.ncbi.nlm.nih.gov/pubmed/34660074
http://dx.doi.org/10.7759/cureus.17875

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