A case report of Bart syndrome

Bart syndrome is a rare condition characterized by epidermolysis bullosa (EB), aplasia cutis (AC), and nail abnormalities. Aplasia cutis congenita type VI was first described in 1966 by Bart et al. This article reports a case of Bart syndrome with ear malformation in a male Afghan newborn. To the au...

Descripción completa

Detalles Bibliográficos
Autores principales: Sharif, Seyed Amirabbas, Mohammadzadeh, Alieh, Heidari, Mohammad Mahdi, Por, Rasoul Etesam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293584/
https://www.ncbi.nlm.nih.gov/pubmed/37384233
http://dx.doi.org/10.1002/ccr3.7612
_version_ 1785063019558993920
author Sharif, Seyed Amirabbas
Mohammadzadeh, Alieh
Heidari, Mohammad Mahdi
Por, Rasoul Etesam
author_facet Sharif, Seyed Amirabbas
Mohammadzadeh, Alieh
Heidari, Mohammad Mahdi
Por, Rasoul Etesam
author_sort Sharif, Seyed Amirabbas
collection PubMed
description Bart syndrome is a rare condition characterized by epidermolysis bullosa (EB), aplasia cutis (AC), and nail abnormalities. Aplasia cutis congenita type VI was first described in 1966 by Bart et al. This article reports a case of Bart syndrome with ear malformation in a male Afghan newborn. To the authors' knowledge, this is the first case of Bart syndrome reported in an Afghan family.
format Online
Article
Text
id pubmed-10293584
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-102935842023-06-28 A case report of Bart syndrome Sharif, Seyed Amirabbas Mohammadzadeh, Alieh Heidari, Mohammad Mahdi Por, Rasoul Etesam Clin Case Rep Case Report Bart syndrome is a rare condition characterized by epidermolysis bullosa (EB), aplasia cutis (AC), and nail abnormalities. Aplasia cutis congenita type VI was first described in 1966 by Bart et al. This article reports a case of Bart syndrome with ear malformation in a male Afghan newborn. To the authors' knowledge, this is the first case of Bart syndrome reported in an Afghan family. John Wiley and Sons Inc. 2023-06-26 /pmc/articles/PMC10293584/ /pubmed/37384233 http://dx.doi.org/10.1002/ccr3.7612 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sharif, Seyed Amirabbas
Mohammadzadeh, Alieh
Heidari, Mohammad Mahdi
Por, Rasoul Etesam
A case report of Bart syndrome
title A case report of Bart syndrome
title_full A case report of Bart syndrome
title_fullStr A case report of Bart syndrome
title_full_unstemmed A case report of Bart syndrome
title_short A case report of Bart syndrome
title_sort case report of bart syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293584/
https://www.ncbi.nlm.nih.gov/pubmed/37384233
http://dx.doi.org/10.1002/ccr3.7612
work_keys_str_mv AT sharifseyedamirabbas acasereportofbartsyndrome
AT mohammadzadehalieh acasereportofbartsyndrome
AT heidarimohammadmahdi acasereportofbartsyndrome
AT porrasouletesam acasereportofbartsyndrome
AT sharifseyedamirabbas casereportofbartsyndrome
AT mohammadzadehalieh casereportofbartsyndrome
AT heidarimohammadmahdi casereportofbartsyndrome
AT porrasouletesam casereportofbartsyndrome

Ejemplares similares