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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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| Gepubliceerd in: | Case Rep Dermatol |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
S. Karger AG
2017
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5624250/ https://ncbi.nlm.nih.gov/pubmed/29033814 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000478889 |
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