Aplasia Cutis Congenita with Fetus Papyraceus: A Rare Case Report
Aplasia cutis congenita is a rare disorder, characterized by the absence of skin tissue at birth. Most commonly occurs as a solitary cutaneous defect on the scalp. It can be classified into 9 phenotypes according to the Frieden’s Classification System. We report a clinical case of a newborn, who was...
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| Outros Autores: | , |
| Formato: | article |
| Idioma: | eng |
| Publicado em: |
2020
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| Texto completo: | https://doi.org/10.25754/pjp.2020.18256 |
| País: | Portugal |
| Oai: | oai:ojs.revistas.rcaap.pt:article/18256 |