Cargando…
ALCAPA Presents in an Adult with Exercise Intolerance but Preserved Cardiac Function
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly that usually manifests as severe left-sided heart failure and mitral valve insufficiency during the first one to two months of life. The majority of these cases die in infancy if not correcte...
Autores principales: | Liu, Yan, Miller, Beth W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007788/ https://www.ncbi.nlm.nih.gov/pubmed/24826255 http://dx.doi.org/10.1155/2012/471759 |
Ejemplares similares
-
Anatomic correction of ALCAPA in an adult presenting with sudden cardiac death
por: Simry, Walid, et al.
Publicado: (2015) -
ALCAPA in an Octogenarian Woman: An Enigma
por: Sinha, Santosh Kumar, et al.
Publicado: (2015) -
Adult ALCAPA: from histological picture to clinical features
por: Kubota, Hiroshi, et al.
Publicado: (2020) -
ALCAPA in adult asymptomatic patient: A case report
por: Talkhatova, Sandugash, et al.
Publicado: (2023) -
Sudden Cardiac Arrest in an Adult with Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): Case Report
por: Prandi, Francesca Romana, et al.
Publicado: (2022)