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Scalp-Ear-Nipple Syndrome: A Case Report
The scalp-ear-nipple (SEN) syndrome is an infrequent congenital disease. Its main features are scalp defects, malformed ears, and absence of nipples. Most of the reported cases are autosomal dominant. We report on a patient suffering SEN syndrome with possible autosomal recessive inheritance. It is...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934383/ https://www.ncbi.nlm.nih.gov/pubmed/24660003 http://dx.doi.org/10.1155/2014/785916 |
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author | Morales-Peralta, Estela Andrés, Vivian Campillo Betancourt, Dainé |
author_facet | Morales-Peralta, Estela Andrés, Vivian Campillo Betancourt, Dainé |
author_sort | Morales-Peralta, Estela |
collection | PubMed |
description | The scalp-ear-nipple (SEN) syndrome is an infrequent congenital disease. Its main features are scalp defects, malformed ears, and absence of nipples. Most of the reported cases are autosomal dominant. We report on a patient suffering SEN syndrome with possible autosomal recessive inheritance. It is concluded that SEN syndrome should be recognized as an entity with genetic heterogeneity once there is evidence of different genetic manner of inheritance described in this disease. |
format | Online Article Text |
id | pubmed-3934383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39343832014-03-23 Scalp-Ear-Nipple Syndrome: A Case Report Morales-Peralta, Estela Andrés, Vivian Campillo Betancourt, Dainé Case Rep Med Case Report The scalp-ear-nipple (SEN) syndrome is an infrequent congenital disease. Its main features are scalp defects, malformed ears, and absence of nipples. Most of the reported cases are autosomal dominant. We report on a patient suffering SEN syndrome with possible autosomal recessive inheritance. It is concluded that SEN syndrome should be recognized as an entity with genetic heterogeneity once there is evidence of different genetic manner of inheritance described in this disease. Hindawi Publishing Corporation 2014 2014-02-09 /pmc/articles/PMC3934383/ /pubmed/24660003 http://dx.doi.org/10.1155/2014/785916 Text en Copyright © 2014 Estela Morales-Peralta et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Morales-Peralta, Estela Andrés, Vivian Campillo Betancourt, Dainé Scalp-Ear-Nipple Syndrome: A Case Report |
title | Scalp-Ear-Nipple Syndrome: A Case Report |
title_full | Scalp-Ear-Nipple Syndrome: A Case Report |
title_fullStr | Scalp-Ear-Nipple Syndrome: A Case Report |
title_full_unstemmed | Scalp-Ear-Nipple Syndrome: A Case Report |
title_short | Scalp-Ear-Nipple Syndrome: A Case Report |
title_sort | scalp-ear-nipple syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934383/ https://www.ncbi.nlm.nih.gov/pubmed/24660003 http://dx.doi.org/10.1155/2014/785916 |
work_keys_str_mv | AT moralesperaltaestela scalpearnipplesyndromeacasereport AT andresvivian scalpearnipplesyndromeacasereport AT campillobetancourtdaine scalpearnipplesyndromeacasereport |