Congenital Aplasia Cutis. A Series of Three Cases
Congenital aplasia cutis is a rare and heterogeneous disorder, with an estimated incidence of 1-3 cases per 10,000 births. It can appear in isolation or as part of several polymalformative syndromes, observing autosomal recessive and autosomal dominant inheritance patterns. Its treatment is controve...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | Spanish |
| Published: |
Universidad de las Ciencias Médicas de Cienfuegos
2021-03-01
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| Series: | Revista Finlay |
| Subjects: | |
| Online Access: | https://revfinlay.sld.cu/index.php/finlay/article/view/958 |
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