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

1p36 deletion syndrome is a common terminal chromosomal deletion syndrome in humans. It is caused by the deletion of genetic material from a specific region in the short arm of chromosome 1. Symptoms range from seizure disorders, abnormalities of tone, visual and auditory disturbances. Cardiac abnor...

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Detalles Bibliográficos
Autores principales: Ogbuji, Chukwunonye O, Ortega, Lucio E, Ward, Haven, Ugochukwu, Nzubechukwu, Donthula, Rakesh, Alapati, Srilatha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590472/
https://www.ncbi.nlm.nih.gov/pubmed/37872928
http://dx.doi.org/10.7759/cureus.45746

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590472/
https://www.ncbi.nlm.nih.gov/pubmed/37872928
http://dx.doi.org/10.7759/cureus.45746

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