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Newborn with a solitary hairless skin defect on the scalp vertex
Aplasia cutis congenita is a rare congenital disorder usually presenting as an isolated lesion on the scalp that may be associated with genetic syndromes and congenital anomalies. Therefore, it is important to be aware of this syndrome.
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| Publicado no: | Clin Case Rep |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6878089/ https://ncbi.nlm.nih.gov/pubmed/31788305 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.2468 |
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