Neuroimaging features in Wolfram syndrome type 1

被引：0
|
作者：
Sameer Peer
Naveen Kumar Bhardwaj
Arvinder Wander
机构：
[1] All India Institute of Medical Sciences, Department of Radiodiagnosis
[2] All India Institute of Medical Sciences,Department of Pediatrics
[3] All India Institute of Medical Sciences,Department of Pediatrics
来源：
Neurological Sciences | 2024年 / 45卷
关键词：
Wolfram syndrome type 1; Acronym DIDMOAD; Vestibulocochlear dysplasia;
D O I：
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中图分类号：
学科分类号：
摘要：
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.
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页码：2943 / 2944
页数：1
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