A case of hypohidrotic ectodermal dysplasia

J Dermatol. 1999 Jan;26(1):44-7. doi: 10.1111/j.1346-8138.1999.tb03508.x.

Abstract

Hypohidrotic ectodermal dysplasia (HED) is a rare, hereditary, congenital disease that affects several ectodermal structures. It is characterised by the following: anhidrosis or hypohidrosis, dental abnormalities, hypotrichosis, and a characteristic facies. The face shows prominent frontal bosses, supraorbital ridges and depressed bridges. We experienced a case of hypohidrotic ectodermal dysplasia in a 43-year-old male who had four characteristic features. A skin biopsy from the palm showed a total absence of the eccrine glands. The diagnosis was made on the basis of clinical features and skin biopsy findings.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Eccrine Glands / pathology
  • Ectodermal Dysplasia* / pathology
  • Humans
  • Male
  • Skin / pathology