Incontinentia pigmenti (Bloch–Siemens syndrome)

被引：1

作者：

Yaqin Zhang

Venkatesh Pyla

Xianling Cong

机构：

[1] The Second Hospital of Jilin University,Department of Dermatology and Venereology

[2] China–Japan Union Hospital of Jilin University,Department of Dermatology and Venereology

来源：

European Journal of Pediatrics | 2013年 / 172卷

关键词：

Incontinentia pigmenti;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Incontinentia pigmenti (IP) is an uncommon X-linked dominant genodermatosis. It affects predominantly females and is lethal in utero in male fetuses. We herein report a baby girl born with blisters on trunk and limbs. The diagnosis of IP was based on clinical findings and on histopathological analysis of biopsy specimen.

引用

页码：1137 / 1138

页数：1

共 11 条

[1]

Nogueira A(2009)Vesicular rash in a newborn Incontinentia pigmenti Indian J Dermatol Venereol Leprol 75 330-681

[2]

Lisboa C(2012)NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: a new disease association Lupus 2 675-1735

[3]

Eloy C(2012)Genodermatoses caused by genetic mosaicism Eur J Pediatr 171 1725-undefined

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