Wolfram syndrome type 1: a case series

BACKGROUND: Wolfram syndrome (WS) is a rare autosomal recessive multisystem neurodegenerative disease characterized by non-autoimmune insulin-dependent diabetes mellitus, optic atrophy, sensorineural deafness, and diabetes as the main features. Owing to clinical phenotypic heterogeneity, the misdiag...

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Detalles Bibliográficos
Autores principales: Du, Danyang, Tuhuti, Aihemaitijiang, Ma, Yanrong, Abuduniyimu, Munila, Li, Suli, Ma, Guoying, Zynat, Jazyra, Guo, Yanying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652474/
https://www.ncbi.nlm.nih.gov/pubmed/37974252
http://dx.doi.org/10.1186/s13023-023-02938-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652474/
https://www.ncbi.nlm.nih.gov/pubmed/37974252
http://dx.doi.org/10.1186/s13023-023-02938-5

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