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一名日本患者出现多发型对称性脂肪瘤病的肌阵挛性癫痫伴破碎红纤维综合征。

MERRF syndrome presenting with multiple symmetric lipomatosis in a Japanese patient.

作者信息

Kobayashi Junpei, Nagao Masahiro, Miyamoto Kazuhito, Matsubara Shiro

机构信息

Department of Neurology, Tokyo Metropolitan Neurological Hospital.

出版信息

Intern Med. 2010;49(5):479-82. doi: 10.2169/internalmedicine.49.2996. Epub 2010 Mar 1.

Abstract

Myoclonic epilepsy with ragged red fibers (MERRF), also called Fukuhara's disease, is sometimes accompanied by the rare symptom of multiple symmetric lipomatosis (MSL). MSL associated with MERRF has been reported mainly in Caucasians; such cases have not been reported in Japanese patients. We report the case of a 59-year-old Japanese woman with MERRF syndrome associated with A-->G substitution at nucleotide 8,344 of mtDNA. This case suggests that differences in lifestyle and gene polymorphism among races may be related to the prevalence of MSL due to mitochondrial abnormality, and that mitochondrial abnormalities should be considered as a cause of MSL even in Japanese patients.

摘要

肌阵挛性癫痫伴破碎红纤维病(MERRF),也称为福原病,有时会伴有罕见的多发性对称性脂肪瘤病(MSL)症状。与MERRF相关的MSL主要在白种人中报道;日本患者中尚未有此类病例报告。我们报告了一例59岁日本女性患有与线粒体DNA(mtDNA)第8344位核苷酸A→G替换相关的MERRF综合征。该病例表明,不同种族间生活方式和基因多态性的差异可能与线粒体异常导致的MSL患病率有关,并且即使在日本患者中,线粒体异常也应被视为MSL的一个病因。

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