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.
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页码：1137 / 1138
页数：1
相关论文
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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