FAMILIAL OCCURRENCE OF KID (KERATITIS, ICHTHYOSIS, DEAFNESS) SYNDROME

被引：46
|
作者：
NAZZARO, V
BLANCHETBARDON, C
LORETTE, G
CIVATTE, J
机构：
[1] HOP ST LOUIS,UNITE RECH DIAGNOST ANTENATAL & DERMATOL,F-75475 PARIS 10,FRANCE
[2] HOP ST LOUIS,MALAD CUTANEES CLIN,F-75475 PARIS 10,FRANCE
[3] HOP TROUSSEAU,SERV DERMATOL,F-75571 PARIS 12,FRANCE
来源：
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY | 1990年 / 23卷 / 02期
关键词：
D O I：
10.1016/0190-9622(90)70229-B
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
Keratitis, ichthyosis, and deafness (KID) syndrome in a mother and her daughter is reported. Both patients showed the typical cutaneous abnormality of papillomatous hyperkeratosis, which gave the skin a grainy, rugose, spiculated appearance, together with keratitis with corneal neovascularization and a neurosensory hearing defect. Treatment with etretinate did not benefit the daughter. The mother had marked keratitis with progressive corneal opacification that required repeated bilateral corneal grafts, which were unsuccessful. This is the second report of hereditary transmission of this disorder. An autosomal dominant mode of inheritance is probable. © 1990, All rights reserved.
引用
收藏
页码：385 / 388
页数：4
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