Perinatal Diagnosis and Management of a Case with Interrupted Aortic Arch, Pulmonary Valve Dysplasia and 22q11.2 Deletion: A Case Report

The 22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion disorder caused by hemizygous microdeletion of the long arm of chromosome 22. It is now known to have a heterogenous presentation that includes multiple additional congenital anomalies and later-onset conditions,...

Descripción completa

Detalles Bibliográficos
Autores principales: Vlădăreanu, Radu, Maier, Călina, Tocariu, Raluca, Șerban, Marcela, Brătilă, Elvira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10608239/
https://www.ncbi.nlm.nih.gov/pubmed/37893556
http://dx.doi.org/10.3390/medicina59101838

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10608239/
https://www.ncbi.nlm.nih.gov/pubmed/37893556
http://dx.doi.org/10.3390/medicina59101838

Ejemplares similares