Data di Pubblicazione:
2022
Abstract:
Wolfram syndrome 1, a rare autosomal recessive neurodegenerative disease, is caused by mutations in the WFS1 gene. It is characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD), and other clinical manifestations such as urological and neurological disorders. Here we described the case of a patient with an atypical late-onset Wolfram syndrome 1 without DI. Our WS1 patient was a c.1620_1622delGTG (p.Trp540del)/c.124 C > T (p.Arg42*) heterozygous compound. The p.Arg42* nonsense mutation was also found in heterozygosity in his sister and niece, both suffering from psychiatric disorders. The p.Arg42* nonsense mutation has never been found in WS1 and its pathogenicity is unclear so far. Our study underlined the need to study a greater number of WS1 cases in order to better understand the clinical significance of many WFS1 variants.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
DIDMOAD, WFS1 mutations, atypical phenotype, wolfram syndrome 1, Humans, Membrane Proteins, Mutation, Pedigree, Diabetes Insipidus, Neurodegenerative Diseases, Wolfram Syndrome
Elenco autori:
Rigoli, Luciana; Caruso, Valerio; Aloi, Concetta; Salina, Alessandro; Maghnie, Mohamad; D'Annunzio, Giuseppe; Lamacchia, Olga; Salzano, Giuseppina; Lombardo, Fortunato; Picca, Giuseppe
Link alla scheda completa:
Pubblicato in: