1p36 Deletion Syndrome and Left Ventricular Non-compaction Cardiomyopathy—Two Cases Report

1p36 deletion is the most common terminal deletion syndrome in humans. Herein, we report two cases, a 5-month-old female and a 14.5-year-old female, both with 1p36 deletion and left ventricular non-compaction cardiomyopathy. They presented with severely depressed left ventricle function and underwen...

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Dades bibliogràfiques
Publicat a:Front Pediatr
Autors principals: Jang, Subin, Taber, Allison, Bateman, Michael G., Steiner, Marie E., Ameduri, Rebecca K., Griselli, Massimo
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2021
Matèries:
Pediatrics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8215124/
https://ncbi.nlm.nih.gov/pubmed/34164357
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2021.653633
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