Radiological Findings of Woodhouse-Sakati Syndrome: Cases Reported From Saudi Arabia

Woodhouse-Sakati syndrome (WSS) is a rare autosomal recessive neurodegenerative genetic disorder caused by mutations in the DCAF17 gene. It primarily manifests with endocrinological symptoms such as hypogonadism, failure to develop secondary sexual characteristics, diabetes, and hypotrichosis. Neuro...

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Detalles Bibliográficos
Autores principales: Alzahrani, Arwa M, Alsuwailem, Lamis O, Alghoraiby, Rinad M, Albadr, Fahad B, Alaseri, Yahya M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522504/
https://www.ncbi.nlm.nih.gov/pubmed/36185913
http://dx.doi.org/10.7759/cureus.28540

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522504/
https://www.ncbi.nlm.nih.gov/pubmed/36185913
http://dx.doi.org/10.7759/cureus.28540

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