Aplasia Cutis Congenita of the Scalp with Bone Defect and Exposed Sagittal Sinus in Trisomy 13 Newborn – a Case Report

BACKGROUND: Aplasia cutis congenita is a heterogeneous disorders group with a rare reported incident of 0.5 to 1 in 10,000 births. ACC can be associated with physical defects or syndrome that may help in diagnosis, prognosis and further evaluation of the patient. Trisomy 13 is one of the most common...

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Detalles Bibliográficos
Autores principales: AlMatrifi, Fisal Rashid, Al-Shammari, Ahmad Ayed, Al Nefily, Raed Mohamed, AlAnazi, Rawan Abdulrahman, Abdulwahab, Abdulrahman Hamed, Ammar, Ahmed Sabry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591249/
https://www.ncbi.nlm.nih.gov/pubmed/37876568
http://dx.doi.org/10.5455/medarh.2023.77.319-322

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