大脑
医学
小脑
异质性
脑干
磁共振成像
先证者
萎缩
桥
巨头症
共济失调
病理
中枢神经系统
解剖
内分泌学
突变
内科学
精神科
放射科
遗传学
生物
基因
作者
Zen Kobayashi,Taiji Tsunemi,Hirotomo Miake,Seiichi Tanaka,Sadakiyo Watabiki,Yuri Morokuma
出处
期刊:Internal Medicine
[The Japanese Society of Internal Medicine]
日期:2005-04-01
被引量:15
标识
DOI:10.2169/internalmedicine.44.328
摘要
A mother and a child with maternally inherited diabetes and deafness (MIDD) showing atrophy of the cerebrum, cerebellum and brainstem on magnetic resonance imaging (MRI) were reported. The proband had slowly progressive cerebellar ataxia and her son had depression. Mitochondrial DNA purified from their leucocytes had the heteroplasmic point mutation at position 3243 (A-->G). Involvement of the central nervous system should be considered in MIDD as well as in other mitochondrial diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI