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一名女性患者的丙酮酸脱氢酶E1α亚基缺乏症:脑损伤产前起源的证据及婴儿痉挛症的可能病因

Pyruvate dehydrogenase E1alpha subunit deficiency in a female patient: evidence of antenatal origin of brain damage and possible etiology of infantile spasms.

作者信息

Wada Naoko, Matsuishi Toyojiro, Nonaka Michiko, Naito Etsuo, Yoshino Makoto

机构信息

Department of Pediatrics and Child Health, Kurume University School of Medicine, 67 Asahi-machi, 830-0011, Kurume, Japan.

出版信息

Brain Dev. 2004 Jan;26(1):57-60. doi: 10.1016/s0387-7604(03)00072-x.

DOI:10.1016/s0387-7604(03)00072-x
PMID:14729417
Abstract

Enlargement of the lateral ventricles and atrophy of the brain were documented ultrasonographically in utero at as early as 28th week of gestation in a female patient with lactic acidosis due to deficiency of the pyruvate dehydrogenase E1alpha subunit, demonstrating that the changes characteristic of this disease can occur antenatally. The mechanism of infantile spasms in this disease may be linked to mosaicism of the brain cells involving the normal enzyme and the mutant enzyme.

摘要

早在妊娠28周时,对一名因丙酮酸脱氢酶E1α亚基缺乏导致乳酸酸中毒的女性患者进行子宫内超声检查,发现其侧脑室扩大和脑萎缩,这表明该疾病的特征性变化可在产前发生。该疾病中婴儿痉挛的机制可能与涉及正常酶和突变酶的脑细胞镶嵌现象有关。

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