Anais Brasileiros de Dermatologia (Apr 2014)

Syndrome in Question

  • Vanessa Mello Tonolli,
  • Hamilton Ometto Stolf,
  • Cláudio Sampieri Tonello,
  • Rafaelle Batistella Pires,
  • Luciana Patricia Fernandes Abbade

DOI
https://doi.org/10.1590/abd1806-4841.20142806
Journal volume & issue
Vol. 89, no. 2
pp. 363 – 364

Abstract

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Hay-Wells syndrome or AEC (Ankyloblepharon, Ectodermal dysplasia and Cleft lip and palate syndrome) is a rare ectodermal disorder. The treatment is aimed to prevent clinical complications. We describe the case of a four-month old male patient with erosions on the scalp, trunk and arms, trachyonychia, deformity of the ears, micropenis, cleft palate, decreased eyebrow and eyelash hairs, in addition to antecedents of surgical correction of ankyloblepharon. The importance of the correct diagnosis is emphasized, besides the investigation of the associated diseases, treatment of complications and genetic counseling of the parents.

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