Keratitis, ichthyosis, and deafness (KID) syndrome in half sibs

被引：22

作者：

Kone-Paut, I ^{[1
]}

Hesse, S ^{[1
]}

Palix, C ^{[1
]}

Rey, R ^{[1
]}

Remediani, K ^{[1
]}

Garnier, JM ^{[1
]}

Berbis, P ^{[1
]}

机构：

[1] Hop Nord, Dept Pediat, F-13915 Marseille, France

来源：

PEDIATRIC DERMATOLOGY | 1998年 / 15卷 / 03期

关键词：

D O I：

10.1046/j.1525-1470.1998.1998015219.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

The keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of the ectoderm characterized by diffuse hyperkeratotic erythroderma, keratitis with neovascularization of the cornea, and severe neurosensory hearing loss, A familiar occurrence of this syndrome has been mentioned in four reports including three of vertical transmission and one of two affected sisters born from consanguineous, unaffected parents. We report far the first time a familial case of KID syndrome in two half siblings born to the same unaffected mother, This new observation allows us to propose various hypotheses about its mode of inheritance.

引用

页码：219 / 221

页数：3

共 10 条

[1] ICHTHYOSIFORM DERMATOSIS, KERATITIS, AND DEAFNESS [J].