Results 1 to 10 of about 200,194 (156)

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   +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   +3 more sources

Lithium-induced Ebstein’s Anomaly

open access: yesHeart Views
Ebstein’s anomaly (EA) is a rare congenital cardiac defect that occurs when the tricuspid valve leaflets fail to delaminate from the ventricular myocardium, they adhere to the underlying myocardium. Multiple etiologies such as genetic mutation in NKX2-5,
Vijaykumar Gupta   +3 more
doaj   +3 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   +4 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

Complete surgical correction of tetralogy of Fallot with Ebstein’s anomaly [PDF]

open access: yesAnnals of Pediatric Cardiology
Association of Ebstein’s anomaly of tricuspid valve (TV) with tetralogy of Fallot (TOF) is extremely rare. Their coexistence is unique as they modify each other’s physiology.
Zarin S. Rangwala   +4 more
doaj   +2 more sources

Cervical Epidural Anaesthesia in a Patient with Ebstein’s Anomaly requiring Total Thyroidectomy [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2023
Ebstein’s anomaly is a congenital malformation of the tricuspid valve with myopathy of the right ventricle leading to dilatation and atrialisation of the right ventricle, with varying degrees of malformation along with restriction of diastolic filling of
Geetha Soundarya Udayakumar   +1 more
doaj   +1 more source

How to manage Ebstein’s Anomaly in Pregnancy: A Literature Review with Case Study [PDF]

open access: yesJournal of Health Sciences and Surveillance System, 2022
Background: Ebstein’s anomaly (EA) is a congenital heart defect that causes cyanosis and arrhythmia. The treating physician has difficulty when it comes to pregnant women since patients frequently reach reproductive age.
Alireza Nematollahi   +3 more
doaj   +1 more source

Report of persistent left superior vena cava associated with Ebstein’s anomaly of tricuspid valve [PDF]

open access: yesARYA Atherosclerosis, 2021
BACKGROUND: Ebstein’s anomaly is one of the challenging congenital heart diseases (CHDs) that is presented with different anatomical and clinical symptoms.
Zahra Khajali, Maryam Aliramezany
doaj   +1 more source

Tatalaksana Anestesi pada Ebstein’s Anomaly yang menjalani Cone Procedure

open access: yesJAI (Jurnal Anestesiologi Indonesia), 2023
Latar Belakang: Ebstein’s anomaly adalah kelainan kongenital yang ditandai dengan malformasi dan perpindahan apikal dari daun katup trikuspid. Pasien datang dengan rentang umur yang luas dari neonatus hingga dewasa dengan berbagai presentasi klinis mulai
Mahendra Dwi Aditya Lopulalan   +1 more
doaj   +1 more source

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