Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1

Wolfram syndrome 1 is a rare, autosomal recessive, neurodegenerative, progressive disorder. Insulin-dependent, non-autoimmune diabetes mellitus and bilateral progressive optic atrophy are both sensitive and specific criteria for clinical diagnosis. The leading cause of death is central respiratory f...

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Detalles Bibliográficos
Autores principales: Salzano, Giuseppina, Rigoli, Luciana, Valenzise, Mariella, Chimenz, Roberto, Passanisi, Stefano, Lombardo, Fortunato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744633/
https://www.ncbi.nlm.nih.gov/pubmed/35010780
http://dx.doi.org/10.3390/ijerph19010520

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744633/
https://www.ncbi.nlm.nih.gov/pubmed/35010780
http://dx.doi.org/10.3390/ijerph19010520

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