Journal of Clinical and Diagnostic Research (Sep 2013)

Hereditary Hypohidrotic Ectodermal Dysplasia: Report of a Rare Case

  • Geetha Paramkusam,
  • Venkateswarlu Meduri,
  • Lakshmi Kavitha Nadendla,
  • Namratha Shetty

DOI
https://doi.org/10.7860/JCDR/2013/5757.3409
Journal volume & issue
Vol. 7, no. 9
pp. 2074 – 2075

Abstract

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Hereditary Hypohidrotic Ectodermal Dysplasia (HHED), an X-linked, recessive, Mendelian character, is seen usually in males and it is inherited through female carriers. It is characterised by congenital dysplasia of one or more ectodermal structures and it is manifested by hypohidrosis, hypotrichosis and hypodontia. It results from abnormal morphogenesis of cutaneous and oral embryonic ectoderm. Here, we are presenting a rare case of HHED in a 19 year female with classic features of this condition.

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