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.

Detalles Bibliográficos
Autores principales: Koumaki, Dimitra, Koumaki, Vasiliki, Boumpoucheropoulos, Sotirios, Baltaga, Ludmila, Bitados, Panagiotis, Katoulis, Alexander, Krasagakis, Konstantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Clinical Image
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878089/
https://www.ncbi.nlm.nih.gov/pubmed/31788305
http://dx.doi.org/10.1002/ccr3.2468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878089/
https://www.ncbi.nlm.nih.gov/pubmed/31788305
http://dx.doi.org/10.1002/ccr3.2468

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