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

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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Autores principales: Valentina Lodato, Valeria Orlando, Viola Alesi, Silvia Di Tommaso, Mario Bengala, Giovanni Parlapiano, Elisa Agnolucci, Marianna Cicenia, Federica Calì, Maria Cristina Digilio, Fabrizio Drago, Antonio Novelli, Anwar Baban
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
1p36 deletion syndrome
heart
aortic dilatation
<i>SKI</i>
Diseases of the circulatory (Cardiovascular) system
RC666-701
Acceso en línea:https://doaj.org/article/e66cb9230e3c4788851e8444807e9dd6
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https://doaj.org/article/e66cb9230e3c4788851e8444807e9dd6

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