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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...
Autores principales: | Salzano, Giuseppina, Rigoli, Luciana, Valenzise, Mariella, Chimenz, Roberto, Passanisi, Stefano, Lombardo, Fortunato |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
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 |
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