22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects

Congenital heart diseases represent one of the hallmarks of 22q11.2 deletion syndrome. In particular, conotruncal heart defects are the most frequent cardiac malformations and are often associated with other specific additional cardiovascular anomalies. These findings, together with extracardiac man...

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Detalles Bibliográficos
Autores principales: Putotto, Carolina, Pugnaloni, Flaminia, Unolt, Marta, Maiolo, Stella, Trezzi, Matteo, Digilio, Maria Cristina, Cirillo, Annapaola, Limongelli, Giuseppe, Marino, Bruno, Calcagni, Giulio, Versacci, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222179/
https://www.ncbi.nlm.nih.gov/pubmed/35740709
http://dx.doi.org/10.3390/children9060772

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222179/
https://www.ncbi.nlm.nih.gov/pubmed/35740709
http://dx.doi.org/10.3390/children9060772

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