TAY OR IBIDS SYNDROME - A CASE WITH GROWTH AND MENTAL-RETARDATION, CONGENITAL ICHTHYOSIS AND BRITTLE HAIR

被引:10
作者
BLOMQUIST, HKS
BACK, O
FAGERLUND, M
HOLMGREN, G
STECKSENBLICKS, C
机构
[1] UMEA UNIV HOSP,DEPT DERMATOL,S-90185 UMEA,SWEDEN
[2] UMEA UNIV HOSP,DEPT DIAGNOST RADIOL,S-90185 UMEA,SWEDEN
[3] UMEA UNIV HOSP,DEPT CLIN GENET,S-90185 UMEA,SWEDEN
[4] UMEA UNIV HOSP,DEPT PEDODONT,S-90185 UMEA,SWEDEN
来源
ACTA PAEDIATRICA SCANDINAVICA | 1991年 / 80卷 / 12期
关键词
TAY SYNDROME; COLLODIUM SKIN; CONGENITAL ICHTHYOSIS; BRITTLE HAIR; TRICHOTHIODYSTROPHY; DENTAL ENAMEL DEFECTS; GROWTH RETARDATION; MENTAL RETARDATION; RECURRENT INFECTIONS; CONSANGUINITY; SQUARE-SHAPED VERTEBRAE;
D O I
10.1111/j.1651-2227.1991.tb11817.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
A new, Swedish case with Tay or IBIDS syndrome is presented. The boy had growth and mental retardation, congenital ichthyosis and brittle hair. He was the only child in an uncle-niece marriage. The boy suffered recurrent infections and died at the age of 3 years from pneumonia. Clinical data on 15 cases are presented from a study of the literature.
引用
收藏
页码:1241 / 1245
页数:5
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