Wolfram Syndrome Type 2: A Systematic Review of a Not Easily Identifiable Clinical Spectrum

Background: Wolfram syndrome (WS) is a rare autosomal recessive disorder that is characterized by the presence of diabetes mellitus, optic atrophy and hearing loss, all of which are crucial elements for the diagnosis. WS is variably associated with diabetes insipidus, neurological disorders, urinary...

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Detalles Bibliográficos
Autores principales: Rosanio, Francesco Maria, Di Candia, Francesca, Occhiati, Luisa, Fedi, Ludovica, Malvone, Francesco Paolo, Foschini, Davide Fortunato, Franzese, Adriana, Mozzillo, Enza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776149/
https://www.ncbi.nlm.nih.gov/pubmed/35055657
http://dx.doi.org/10.3390/ijerph19020835

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776149/
https://www.ncbi.nlm.nih.gov/pubmed/35055657
http://dx.doi.org/10.3390/ijerph19020835

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