Hypohidrotic ectodermal dysplasia: A case report: Hipohidrotik ektodermal dysplasia: Bir olgu sunumu

Vagish  Kumar L S

doi:10.5455/GMJ-30-172543

Authors

Vagish Kumar L S Department of Oral Medicine and Radiology, Yenepoya Dental College and Hospital, Yenepoya Research Centre, Yenepoya University

DOI:

https://doi.org/10.5455/GMJ-30-172543

Keywords:

Christ-Siemens Touraine syndrome, ectodermal dysplasia, hypohidrosis, missing teeth

Abstract

Ectodermal dysplasia is a hereditary disorder exhibiting developmental abnormalities of ectodermal structures. Patients with these disorders usually exhibit multiple missing teeth, sparse hair and inability to sweat with other manifestations. Early recognition and treatment by clinicians will prevent development of psychological trauma in patient and gives confidence to the patient. The current article presents a case of a 28 year old male with hypohidrotic ectodermal dysplasia who presented with rare unusual hyperpigmentations.

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