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Type VI Aplasia Cutis Congenita: Bart's Syndrome
Bart's syndrome is characterized by aplasia cutis congenita and epidermolysis bullosa. We present the case of a newborn male who developed blisters on the mucous membranes and the skin following congenital localized absence of skin. Bart's syndrome (BS) is diagnosed clinically based on the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644546/ https://www.ncbi.nlm.nih.gov/pubmed/26609453 http://dx.doi.org/10.1155/2015/549825 |
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author | Kulalı, Ferit Bas, Ahmet Yagmur Kale, Yusuf Celik, Istemi Han Demirel, Nihal Apaydın, Sema |
author_facet | Kulalı, Ferit Bas, Ahmet Yagmur Kale, Yusuf Celik, Istemi Han Demirel, Nihal Apaydın, Sema |
author_sort | Kulalı, Ferit |
collection | PubMed |
description | Bart's syndrome is characterized by aplasia cutis congenita and epidermolysis bullosa. We present the case of a newborn male who developed blisters on the mucous membranes and the skin following congenital localized absence of skin. Bart's syndrome (BS) is diagnosed clinically based on the disorder's unique signs and symptoms but histologic evaluation of the skin can help to confirm the final diagnosis. The patient was managed conservatively with topical antibacterial ointment and wet gauze dressing. Periodic follow-up examinations showed complete healing. We emphasized that it is important to use relatively simple methods for optimal healing without the need for complex surgical interventions. |
format | Online Article Text |
id | pubmed-4644546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-46445462015-11-25 Type VI Aplasia Cutis Congenita: Bart's Syndrome Kulalı, Ferit Bas, Ahmet Yagmur Kale, Yusuf Celik, Istemi Han Demirel, Nihal Apaydın, Sema Case Rep Dermatol Med Case Report Bart's syndrome is characterized by aplasia cutis congenita and epidermolysis bullosa. We present the case of a newborn male who developed blisters on the mucous membranes and the skin following congenital localized absence of skin. Bart's syndrome (BS) is diagnosed clinically based on the disorder's unique signs and symptoms but histologic evaluation of the skin can help to confirm the final diagnosis. The patient was managed conservatively with topical antibacterial ointment and wet gauze dressing. Periodic follow-up examinations showed complete healing. We emphasized that it is important to use relatively simple methods for optimal healing without the need for complex surgical interventions. Hindawi Publishing Corporation 2015 2015-11-01 /pmc/articles/PMC4644546/ /pubmed/26609453 http://dx.doi.org/10.1155/2015/549825 Text en Copyright © 2015 Ferit Kulalı 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 Kulalı, Ferit Bas, Ahmet Yagmur Kale, Yusuf Celik, Istemi Han Demirel, Nihal Apaydın, Sema Type VI Aplasia Cutis Congenita: Bart's Syndrome |
title | Type VI Aplasia Cutis Congenita: Bart's Syndrome |
title_full | Type VI Aplasia Cutis Congenita: Bart's Syndrome |
title_fullStr | Type VI Aplasia Cutis Congenita: Bart's Syndrome |
title_full_unstemmed | Type VI Aplasia Cutis Congenita: Bart's Syndrome |
title_short | Type VI Aplasia Cutis Congenita: Bart's Syndrome |
title_sort | type vi aplasia cutis congenita: bart's syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644546/ https://www.ncbi.nlm.nih.gov/pubmed/26609453 http://dx.doi.org/10.1155/2015/549825 |
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