A Rare Case of an Infant With 1p36 Deletion Syndrome Presenting With Systolic Heart Failure Secondary to Severe Dilated Cardiomyopathy

Author:

Ogbuji Chukwunonye O,Ortega Lucio E,Ward Haven,Ugochukwu Nzubechukwu,Donthula Rakesh,Alapati Srilatha

Publisher

Springer Science and Business Media LLC

Subject

Aerospace Engineering

Reference10 articles.

1. 1p36 deletion syndrome. (2023). Accessed. September 20, 2023: https://rarediseases.info.nih.gov/diseases/6082/chromosome-1p36-deletion-syndrome.

2. Cardiomyopathies in children and systemic disorders when is it useful to look beyond the heart?;Lodato V;J Cardiovasc Dev Dis,2022

3. 1p36 deletion syndrome and left ventricular non-compaction cardiomyopathy-two cases report;Jang S;Front Pediatr,2021

4. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia A;Pediatrics,2008

5. 1p36 deletion syndrome: an update;Jordan VK;Appl Clin Genet,2015

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