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Syndrome in Question()

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...

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Autores principales: Tonolli, Vanessa Mello, Stolf, Hamilton Ometto, Tonello, Cláudio Sampieri, Pires, Rafaelle Batistella, Abbade, Luciana Patricia Fernandes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008080/
https://www.ncbi.nlm.nih.gov/pubmed/24770526
http://dx.doi.org/10.1590/abd1806-4841.20142806
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author Tonolli, Vanessa Mello
Stolf, Hamilton Ometto
Tonello, Cláudio Sampieri
Pires, Rafaelle Batistella
Abbade, Luciana Patricia Fernandes
author_facet Tonolli, Vanessa Mello
Stolf, Hamilton Ometto
Tonello, Cláudio Sampieri
Pires, Rafaelle Batistella
Abbade, Luciana Patricia Fernandes
author_sort Tonolli, Vanessa Mello
collection PubMed
description 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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spelling pubmed-40080802014-05-07 Syndrome in Question() Tonolli, Vanessa Mello Stolf, Hamilton Ometto Tonello, Cláudio Sampieri Pires, Rafaelle Batistella Abbade, Luciana Patricia Fernandes An Bras Dermatol Syndrome in Question 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. Sociedade Brasileira de Dermatologia 2014 /pmc/articles/PMC4008080/ /pubmed/24770526 http://dx.doi.org/10.1590/abd1806-4841.20142806 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Syndrome in Question
Tonolli, Vanessa Mello
Stolf, Hamilton Ometto
Tonello, Cláudio Sampieri
Pires, Rafaelle Batistella
Abbade, Luciana Patricia Fernandes
Syndrome in Question()
title Syndrome in Question()
title_full Syndrome in Question()
title_fullStr Syndrome in Question()
title_full_unstemmed Syndrome in Question()
title_short Syndrome in Question()
title_sort syndrome in question()
topic Syndrome in Question
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008080/
https://www.ncbi.nlm.nih.gov/pubmed/24770526
http://dx.doi.org/10.1590/abd1806-4841.20142806
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