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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...
Autores principales: | Alzahrani, Arwa M, Alsuwailem, Lamis O, Alghoraiby, Rinad M, Albadr, Fahad B, Alaseri, Yahya M |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
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 |
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