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J Ayub Med Coll Abbottabad ; 34(4): 895-897, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36566424

RESUMEN

Ectodermal Dysplasia (ED) is a rare genetic condition characterized by the involvement of ectoderm derivatives such as hair, nail, sweat glands, and teeth. It has many variants, but the two most common ones are hypohidrotic/anhidrotic ectodermal dysplasia and hidrotic ectodermal dysplasia. Herein, we present a case of a 20-year-old female with hypohidrotic ectodermal dysplasia who had anodontia, hypohidrosis, and hypotrichosis, and her condition went unrecognized until she was seen for gastroenteritis at a tertiary care center. This case report will help spread education and awareness regarding such a rare and under-recognized condition. Early diagnosis and intervention help improve the quality of life.


Asunto(s)
Anodoncia , Displasia Ectodermal Anhidrótica Tipo 1 , Displasia Ectodérmica , Humanos , Femenino , Adulto Joven , Adulto , Displasia Ectodermal Anhidrótica Tipo 1/complicaciones , Displasia Ectodermal Anhidrótica Tipo 1/diagnóstico , Calidad de Vida , Displasia Ectodérmica/complicaciones , Displasia Ectodérmica/diagnóstico , Anodoncia/etiología
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