Article
Wolfram Syndrome 1: A Neuropsychiatric Perspective on a Rare Disease.
Genes - 25 Jul 2024
Caruso Valerio, Raia Accursio, Rigoli Luciana
Abstract excerpt
Wolfram syndrome 1 (WS1) is an uncommon autosomal recessive neurological disorder that is characterized by diabetes insipidus, early-onset non-autoimmune diabetes mellitus, optic atrophy, and deafness (DIDMOAD). Other clinical manifestations are neuropsychiatric symptoms, urinary tract alterations, and endocrinological disorders. The rapid clinical course of WS1 results in death by the age of 30. Severe brain...
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