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1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature Review

Background: Monosomy 1p36 syndrome is now considered the most common terminal deletion syndrome, with an estimated incidence of 1 in 5000. Cardiac involvement is well described in the literature mainly in terms of congenital heart defects (CHDs) and cardiomyopathies (CMPs). Few data in the literatur...

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Detalles Bibliográficos
Autores principales:	Lodato, Valentina, Orlando, Valeria, Alesi, Viola, Di Tommaso, Silvia, Bengala, Mario, Parlapiano, Giovanni, Agnolucci, Elisa, Cicenia, Marianna, Calì, Federica, Digilio, Maria Cristina, Drago, Fabrizio, Novelli, Antonio, Baban, Anwar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618808/ https://www.ncbi.nlm.nih.gov/pubmed/34821712 http://dx.doi.org/10.3390/jcdd8110159

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