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
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
收藏
页码:140 / 142
页数:3
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