Neuroimaging features in Wolfram syndrome type 1.
Neurol Sci
; 45(6): 2943-2944, 2024 Jun.
Article
en En
| MEDLINE
| ID: mdl-38291196
ABSTRACT
Wolfram syndrome type 1 is a rare autosomal recessive genetic disorder which is characterized by the co-existence of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness, and hence is also referred to as the acronym DIDMOAD. In this neuroimage, the typical neuroimaging features of a genetically confirmed case of Wolfram syndrome type 1 are presented. The presence of left-sided vestibulocochlear dysplasia is a novel finding in our case which has not been reported previously.
Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Síndrome de Wolfram
/
Neuroimagen
Límite:
Humans
Idioma:
En
Año:
2024
Tipo del documento:
Article