FAMILIAL ECTODERMAL DYSPLASIA WITH SENSORI-NEURAL DEAFNESS AND OTHER ANOMALIES

Abstract
This case report presents the pedigree of a family with hereditary ectodermal dysplasia of the hidrotic type in which various members showed sensori-neural hearing loss, polydactylism, and syndactylism. In addition the affected members showed an elevation of electrolyte concentrations in sweat. This appears to be a new syndrome.