Clinical Spectrum Associated with Wolfram Syndrome Type 1 and Type 2: A Review on Genotype–Phenotype Correlations

Wolfram syndrome is a rare neurodegenerative disorder that is typically characterized by diabetes mellitus and optic atrophy. Other common features are diabetes insipidus and hearing loss, but additional less-frequent findings may also be present. The phenotype spectrum is quite wide, and penetrance...

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Detalles Bibliográficos
Autores principales: Delvecchio, Maurizio, Iacoviello, Matteo, Pantaleo, Antonino, Resta, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124476/
https://www.ncbi.nlm.nih.gov/pubmed/33946243
http://dx.doi.org/10.3390/ijerph18094796

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124476/
https://www.ncbi.nlm.nih.gov/pubmed/33946243
http://dx.doi.org/10.3390/ijerph18094796

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