SCALP-EAR-NIPPLE SYNDROME - ADDITIONAL MANIFESTATIONS

被引:24
作者
EDWARDS, MJ
MCDONALD, D
MOORE, P
RAE, J
机构
[1] TAMWORTH BASE HOSP & HLTH SERV,DEPT GENET COUNSELING,TAMWORTH,AUSTRALIA
[2] TAMWORTH BASE HOSP & HLTH SERV,NEWCASTLE & NO NEW S WALES GENET SERV,TAMWORTH,AUSTRALIA
[3] TAMWORTH BASE HOSP & HLTH SERV,DEPT PAEDIAT,TAMWORTH,AUSTRALIA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 50卷 / 03期
关键词
SCALP APLASIA; SCARRING; ALOPECIA; EAR; NIPPLE; BREAST; SYNDACTYLY; APOCRINE SWEAT GLANDS; DENTAL ABNORMALITIES; AUTOSOMAL DOMINANT;
D O I
10.1002/ajmg.1320500307
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Scalp-ear-nipple (SEN) syndrome is a rare, autosomal dominant condition that causes aplasia cutis congenita of the scalp, alteration of the shape of the external ear, and hypoplasia of the nipple. Women in a new family, the fifth to be described, had virtually complete aplasia of the breast and a small skin dimple without any pigmentation instead of a normal nipple, although other affected women had normal breast and nipple development. Dental changes included widely spaced or missing secondary teeth; the ears were cupped or folded and stood out from the head, axillary apocrine secretion and axillary hair growth were reduced; and finger nails were brittle. There was no generalized abnormality of sweating. Some patients had partial syndactyly of the 3rd and 4th fingers, and complete cutaneous syndactyly of the 2nd and 3rd toes. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:247 / 250
页数:4
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