Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua

被引：21

作者：

Elia, M

Musumeci, SA

Ferri, R

Colamaria, V

Azan, G

Greco, D

Stefanini, MC

机构：

[1] OASI INST RES MENTAL RETARDAT & BRAIN AGING,DEPT PEDIAT,I-94018 TROINA,EN,ITALY

[2] III SERV CHILD NEUROPSYCHIAT,I-37122 VERONA,ITALY

来源：

BRAIN & DEVELOPMENT | 1996年 / 18卷 / 03期

关键词：

Leigh syndrome; COX partial deficit; epilepsia partialis continua;

D O I：

10.1016/0387-7604(95)00126-3

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Epilepsia partialis continua (EPC) has previously been reported in only two patients with Leigh syndrome (LS). We report here a subject in whom LS and partial deficit of cytochrome c oxidase (COX) were associated with EPC. Epilepsy in this subject appeared when neurologic impairment was clearly evident and MRI showed cortical lesions typically associated with congenital lactic acidosis.

引用

页码：207 / 211

页数：5

共 25 条

[1]

AICARDI J, 1992, DIS NERVOUS SYSTEM C, P457

[2]

Bancaud Jean, 1992, P363

[3]

CHEVRIE JJ, 1987, ADV EPILEPTOL, V16, P181

[4]

MATERNALLY INHERITED LEIGH SYNDROME [J].