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：

暂无

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.

引用

页码：2943 / 2944

页数：1

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