Athelia in a female infant heterozygous for anhidrotic ectodermal dysplasia
- 23 April 2008
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 19 (2) , 117-121
- https://doi.org/10.1111/j.1399-0004.1981.tb00680.x
Abstract
The case of a female infant with athelia is reported. Her mother, maternal aunt and grandmother show hypodontia, sparse hair and small breasts associated with mammillary hypoplasia. The clinical features and the results of Minor''s sweat test suggest a heterozygous state of anhidrotic ectodermal dysplasia as the most likely explanation.This publication has 13 references indexed in Scilit:
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