J Korean Pediatr Soc.  1996 Jul;39(7):1005-1009.

Herditary Anhidrotic Ectodermal Dysplasia in Twins

Affiliations
  • 1Department of Pediatrics, EUL JI Medical Center, Seoul, Korea.

Abstract

Hereditary anhidrotic ectodermal Dysplasia is a congenital disease displaying characteristics of anhidrosis, hypotrichosis and dental defect which are caused by developmental anomaly of ectodermal epidermis and its appendages. We experienced two cases of hereditary anhidrotic ectodermal dysplasia in two-year and four-month old twin brothers. These patients suffered from intermittent high fever early in life which brought them to our clinical attention. However the diagnosis of anhidrotic ectodermal dysplasia was not suspected by means physicians who cared the patients previously. The diagnosis was made on the basis of clinical features, and confirmed by starch iodine sweat test and skin biopsy on the palm and axilla. We report the two cases in a twin brothers with brief review of related literatures.

Keyword

Anhidrotic ectodermal dysplasia; Twins

MeSH Terms

Axilla
Biopsy
Diagnosis
Ectoderm
Ectodermal Dysplasia*
Epidermis
Fever
Humans
Hypohidrosis
Hypotrichosis
Iodine
Siblings
Skin
Starch
Sweat
Twins*
Iodine
Starch
Full Text Links
  • KJP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr