L-2-Hydroxyglutaric aciduria presenting as status epilepticus

被引:15
作者
Zafeiriou, DI
Sewell, A
Savvopoulou-Augoustidou, P
Gombakis, N
Katzos, G
机构
[1] Aristotelian Univ Salonika, Dev Ctr A Fokas, Pediat Clin 1, GR-54006 Salonika, Greece
[2] Univ Frankfurt, Dept Pediat, D-6000 Frankfurt, Germany
关键词
L-2-Hydroxyglutaric aciduria; macrocephaly; subcortical leukodystrophy; ataxia; status epilepticus;
D O I
10.1016/S0387-7604(01)00206-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
L-2-Hydroxyglutaric aciduria (L-2-HGA) is a rare organic aciduria with a slowly progressive course regarding CNS involvement. We present a 13.5-year-old female patient who presented at the Emergency Department with a generalized status epilepticus, which promptly responded to intravenous: phenytoin. CT and MRI demonstrated subcortical white matter alterations. The neurological examination revealed mild mental retardation, macrocephaly and ataxic gait with cerebellar signs. Repeated urinary organic acid analysis demonstrated increased excretion of 2-hydroxyglutaric acid which was of the L-configuration. The constellation of macrocephaly in a patient with mental retardation, cerebellar tract involvement and subcortical white matter signal alterations on MRI should alert the physician to the possibility of L-2-HGA. Although rare, epileptic seizures or even status epilepticus can be among the presenting symptoms in organic acidurias with a slow course, such as L-2-HGA. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:255 / 257
页数:3
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