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.

Salvato in:
Dettagli Bibliografici
Pubblicato in:Clin Case Rep
Autori principali: Koumaki, Dimitra, Koumaki, Vasiliki, Boumpoucheropoulos, Sotirios, Baltaga, Ludmila, Bitados, Panagiotis, Katoulis, Alexander, Krasagakis, Konstantinos
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2019
Soggetti:
Clinical Image
Accesso online: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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