Results 1 to 10 of about 3,684 (208)

Antenatal Diagnosis of a Partial Atrioventricular Canal with Ebstein’s Anomaly [PDF]

open access: goldChildren, 2021
The simultaneous occurrence of an atrioventricular canal defect (AVCD) and Ebstein’s anomaly is extremely rare, occurring in less than 0.5% of all patients with AVCD. Only 22 cases are described in the literature.
Gerald Laforest   +4 more
doaj   +4 more sources

Heterozygous nonsense variants in laminin subunit 3α resulting in Ebstein’s anomaly [PDF]

open access: yesHGG Advances, 2023
Summary: Ebstein’s anomaly is a rare congenital heart disease characterized by tricuspid valve downward displacement and is associated with additional cardiac phenotypes such as left ventricle non-compaction.
Zhou Zhou   +12 more
doaj   +2 more sources

Image to Fit the Clinical Picture: Point-of-care Ultrasound Assessment of Ebstein’s Anomaly in Peru [PDF]

open access: yesClinical Practice and Cases in Emergency Medicine, 2020
Ebstein’s anomaly is a congenital heart defect that when left untreated can lead to unique physical exam and ultrasound findings. This case describes a patient who presented with dyspnea and was found to have cyanosis, clubbing, and dilation of right ...
Ashley C. Rider   +2 more
doaj   +3 more sources

A Rare Manifestation of Asymptomatic Ebstein’s Anomaly with Tricuspid Valve Endocarditis [PDF]

open access: yesCase Reports in Cardiology, 2017
Ebstein’s anomaly is a rare congenital heart disease that presents with apical displacement of the septal and posterior leaflets of the tricuspid valve. It has a wide spectrum of clinical presentations and has been shown to manifest itself any time from ...
Carmel Moazez   +3 more
doaj   +3 more sources

Case report of Ebstein’s anomaly in a young female [PDF]

open access: yesSAGE Open Medical Case Reports
Ebstein’s anomaly, also known as Ebstein’s malformation, is a congenital heart defect that occurs in about 0.005% of live births and accounts for 0.3–0.6% of all congenital heart disease.
Rediet Dessalegne   +3 more
doaj   +2 more sources

Pregnancy outcomes in women with Ebstein’s anomaly: data from the Registry of Pregnancy And Cardiac disease (ROPAC) [PDF]

open access: yesOpen Heart, 2023
Objective Ebstein’s anomaly is a rare congenital cardiac condition and data regarding pregnancy outcomes in this patient group are scarce. We evaluated the maternal and perinatal risks of pregnancy in 81 women with Ebstein’s anomaly.Methods The Registry ...
Jolien W Roos-Hesselink   +11 more
doaj   +2 more sources

Rare loss-of-function variants in matrisome genes are enriched in Ebstein’s anomaly [PDF]

open access: yesHGG Advances
Summary: Ebstein’s anomaly, a rare congenital heart disease, is distinguished by the failure of embryological delamination of the tricuspid valve leaflets from the underlying primitive right ventricle myocardium. Gaining insight into the genetic basis of
Zhou Zhou   +7 more
doaj   +2 more sources

Neonatal Ebstein’s Anomaly: Surgical Decision Making [PDF]

open access: yesThe Annals of African Surgery, 2018
Ebstein’s Anomaly (EA) is a rare form of congenital heart disease. Surgical decision-making in neonates is controversial. In developing countries, neonates with Ebstein’s anomaly requiring surgical intervention rarely present to health institutions ...
Awori M, Mutwiri RK, Mutunga WM, Jowi SO
doaj   +3 more sources

An Unusual Case of Tricuspid Stenosis [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2018
Tricuspid stenosis is an uncommon valvular abnormality commonly associated with other valvular lesions. Ebstein's anomaly is a rare congenital heart malformation characterized primarily by abnormalities of the tricuspid valve and right ventricle ...
Sara Ferreira   +6 more
doaj   +4 more sources

Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7 [PDF]

open access: hybrid, 2011
Ebstein's anomaly is a rare congenital heart malformation characterised by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium.
A. F. M. Moorman   +16 more
core   +3 more sources

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