SWEAT TESTING TO IDENTIFY FEMALE CARRIERS OF X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA

被引:12
|
作者
CLARKE, A [1 ]
BURN, J [1 ]
机构
[1] ROYAL VICTORIA INFIRM,DEPT HUMAN GENET,NEWCASTLE TYNE NE2 4AA,ENGLAND
关键词
D O I
10.1136/jmg.28.5.330
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
X linked hypohidrotic ectodermal dysplasia (XHED) affects many epithelial functions, including sweat gland formation. Female carriers who manifest XHED may have defective dentition or a patchy distribution of sweating or both, as determined by starch and iodine sweat testing. Such sweat testing can be useful in assigning carrier status to at risk females in XHED families, and in obtaining an accurate diagnosis for isolated females who present with features of ectodermal dysplasia. The advantages of diagnosing female carriers of XHED include the optimisation of neonatal and paediatric care for affected male infants, who may be at substantial risk of death in infancy.
引用
收藏
页码:330 / 333
页数:4
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