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一名患有克兰费尔特综合征男婴的色素失禁症:病例报告及文献综述

Incontinentia pigmenti in a male infant with Klinefelter syndrome: a case report and review of the literature.

作者信息

Buinauskaite Evelina, Buinauskiene Jurate, Kucinskiene Vesta, Strazdiene Dale, Valiukeviciene Skaidra

机构信息

Department of Skin and Venereal Diseases, Kaunas University of Medicine, Kaunas, Lithuania.

出版信息

Pediatr Dermatol. 2010 Sep-Oct;27(5):492-5. doi: 10.1111/j.1525-1470.2010.01261.x. Epub 2010 Aug 27.

Abstract

Incontinentia pigmenti, also known as Bloch-Sulzberger syndrome, is a hereditary, X-linked dominant disorder characterized by abnormalities of skin, hair, teeth, eyes, and the central nervous system. It is classically considered a male-lethal disorder leading to recurrent miscarriages of male fetuses. We report a rare case of a surviving baby boy with the classic clinical features of incontinentia pigmenti that can be explained by Klinefelter syndrome.

摘要

色素失禁症,又称布洛赫-苏尔茨贝格综合征,是一种遗传性X连锁显性疾病,其特征为皮肤、毛发、牙齿、眼睛及中枢神经系统异常。传统上认为这是一种男性致死性疾病,可导致男性胎儿反复流产。我们报告了一例罕见的存活男婴病例,其具有色素失禁症的典型临床特征,这可用克兰费尔特综合征来解释。

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