A Case of Aplasia Cutis Congenita Type VI: Bart Syndrome

Aplasia cutis congenita type VI, also known as Bart syndrome, is a rare genetic mechanobullous disorder characterized by congenital localized absence of skin, mucocutaneous blistering lesions, and nail abnormalities. We present the case of a 4-h-old male newborn who presented with complete absence o...

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Detalles Bibliográficos
Autores principales: Alfayez, Yasmin, Alsharif, Sahar, Santli, Adel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2017
Materias:
Single Case
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624250/
https://www.ncbi.nlm.nih.gov/pubmed/29033814
http://dx.doi.org/10.1159/000478889

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624250/
https://www.ncbi.nlm.nih.gov/pubmed/29033814
http://dx.doi.org/10.1159/000478889

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