Cerebellar vermis hypoplasia and bilateral basal ganglia calcification in maternally inherited diabetes and deafness

被引:0
|
作者
Li, Jie [1 ]
He, Ni [1 ]
机构
[1] Peoples Hosp Deyang City, Dept Neurol, 173 North Taishan Rd, Deyang 618000, Sichuan, Peoples R China
关键词
Maternally inherited diabetes and deafness; Basal ganglia calcification; Cerebellar vermis hypoplasia; Mitochondrial; Genetic;
D O I
10.1007/s10072-022-06529-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Maternally inherited diabetes and deafness (MIDD) is a rare diabetic syndrome mainly caused by a point mutation in the mitochondrial DNA. It affects up to 1% of patients with diabetes but is often unrecognized by physicians. We report a case of MIDD in a 29-year-old man with coexisting imaging of cerebellar vermis hypoplasia and bilateral basal ganglia calcification.
引用
收藏
页码:1469 / 1470
页数:2
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