Ectodermal Dysplasia and Neurosensory Deafness

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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Other congenital malformations

OMIM Number

224800

Mode of Inheritance

Autosomal recessive

Description

This is an extremely rare disorder, characterized by Hidrotic ectodermal dysplasia and sensorineural hearing loss. So far, the association has only been reported in a single Lebanese family. 

Epidemiology in the Arab World

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Other Reports

Lebanon

Mikaelian et al. (1970) described an affected brother and sister, born to cinsanguineous parents. Both patients had hidrotic ectodermal dysplasia, sensorineural hearing loss, and contracture of the fifth fingers.  

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