CONGENITAL ICHTHYOSIS PRECEDING NEUROLOGIC SYMPTOMS IN 2 SIBS WITH TYPE-2 GAUCHER-DISEASE

被引:24
作者
FUJIMOTO, A
TAYEBI, N
SIDRANSKY, E
机构
[1] NIMH,CLIN NEUROSCI BRANCH,BETHESDA,MD 20892
[2] UNIV SO CALIF,SCH MED,DEPT PEDIAT,DIV GENET,LOS ANGELES,CA 90033
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 59卷 / 03期
关键词
COLLODION BABY; GLUCOCERBROSIDASE DEFICIENCY; EPIDERMAL ABNORMALITIES;
D O I
10.1002/ajmg.1320590315
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe 2 sibs who presented with ichthyotic skin at birth and subsequently developed neurologic manifestations of type 2 Gaucher disease. Type 2 Gaucher patients with and without ichthyosis manifest ultrastructural and biochemical abnormalities in the epidermis. The 2 patients described here clearly demonstrate that epidermal involvement in type 2 Gaucher disease may precede neurologic symptoms and substantiate the prognostic significance of early skin abnormalities in Gaucher patients. Gaucher disease should be considered in the differential diagnosis of congenital ichthyosis, even if the scaling resolves spontaneously. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:356 / 358
页数:3
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