Wolfram Syndrome (Diabetes Insipidus, Diabetes, Optic Atrophy, and Deafness): Clinical and genetic study

OBJECTIVE—Wolfram syndrome is an autosomal recessive neurodegenerative disorder characterized by diabetes insipidus, diabetes (nonautoimmune), optic atrophy, and deafness (a set of conditions referred to as DIDMOAD). The WFS1 gene is located on the short arm of chromosome 4. Wolfram syndrome prevale...

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Detalles Bibliográficos
Autores principales: d'Annunzio, Giuseppe, Minuto, Nicola, D'Amato, Elena, de Toni, Teresa, Lombardo, Fortunato, Pasquali, Lorenzo, Lorini, Renata
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2008
Materias:
Clinical Care/Education/Nutrition/Psychosocial Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518337/
https://www.ncbi.nlm.nih.gov/pubmed/18566338
http://dx.doi.org/10.2337/dc08-0178

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518337/
https://www.ncbi.nlm.nih.gov/pubmed/18566338
http://dx.doi.org/10.2337/dc08-0178

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