Adult-onset Leigh's disease: A rare entity

被引：9

作者：

Jabeen, Shaik Afshan ^{[1
]}

Sandeep, G. ^{[1
]}

Mridula, Kandadai Rukmini ^{[1
]}

Meena, Angamuttu Kanikannan ^{[1
]}

Borgohain, Rupam ^{[1
]}

Sundaram, Challa ^{[2
]}

机构：

[1] Nizams Inst Med Sci, Dept Neurol, Millennium Block, Hyderabad 50082, Andhra Pradesh, India

[2] Nizams Inst Med Sci, Dept Pathol, Hyderabad, Andhra Pradesh, India

来源：

ANNALS OF INDIAN ACADEMY OF NEUROLOGY | 2016年 / 19卷 / 01期

关键词：

Adult onset; brain stem hyperintensities; bulbar palsy; Leigh's disease; serum lactate;

D O I：

10.4103/0972-2327.175437

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Leigh syndrome (LS) is a heterogeneous familial or sporadic neurodegenerative disorder. It is typically seen in infancy or childhood, although rare cases of adult onset have been described. The authors describe a 37-year-old woman who presented with protracted gastrointestinal symptoms followed by acute brain stem syndrome with severe metabolic acidosis and who subsequently showed dramatic clinical and neuroradiological improvement.

引用

页码：140 / 142

页数：3

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