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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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| Izdano u: | Case Rep Dermatol |
|---|---|
| Glavni autori: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
S. Karger AG
2017
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| Teme: | |
| Online pristup: | 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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