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Cardiac Laterality: Surgical Results of Right Atrial Isomerism [PDF]

open access: greenDiseases (Basel, Switzerland), 2023
Right atrial isomerism (RAI) is a complex entity with varying diagnostic and treatment outcomes due to its rarity. Treatment options range from palliative to corrective surgeries, resulting in heterogeneous outcomes.
Diego B Ortega-Zhindón   +2 more
exaly   +6 more sources

Senning Procedure for Physiological Atrial Inversion With Left Atrial Isomerism [PDF]

open access: yesJACC: Case Reports, 2019
We present the case of an infant with left atrial isomerism with complex pulmonary and systemic venous connections that resulted in physiological parallel circulation in the setting of ventriculoarterial concordance who was surgically treated using the ...
Bibhuti B Das   +2 more
exaly   +6 more sources

Outcomes of the Surgical Management of Atrial Isomerism and Functional Single Ventricle: A Single-Centered Cohort From China [PDF]

open access: yesFrontiers in Cardiovascular Medicine, 2021
Objectives: The management of atrial isomerism with complex congenital heart disease remains challenging. Experience has been largely obtained in advanced countries. The clinical diversity is greater in China.
Jia Li, Xin-Xin Chen, Cao Fan
exaly   +4 more sources

Strategy of delayed repair of total anomalous pulmonary venous connection in right atrial isomerism and functional single ventricleCentral MessagePerspective [PDF]

open access: goldJTCVS Open, 2022
Objective: Repair of total anomalous pulmonary venous connection (TAPVC) in neonates with right atrial isomerism and functional single ventricle is challenging.
Eiri Kisamori, MD   +6 more
doaj   +4 more sources

Successful preterm cesarean delivery in a woman with right atrial isomerism: a case report [PDF]

open access: yesBMC Pregnancy and Childbirth
Background Right atrial isomerism is a rare condition marked by congenital splenic aplasia and associated cardiovascular and visceral malformations. The etiology of this condition remains unclear.
Yuru He, Qiulei Wu, Ying Zhu, Geqing Xia
doaj   +2 more sources

Antenatal diagnosis of left atrial isomerism and heterotaxy syndrome in fetus with Meckel-Gruber syndrome

open access: greenTürk Kardiyoloji Derneği Arşivi, 2014
We aimed to present a fetus with Meckel-Gruber syndrome (MKS) who had left atrial isomerism, heterotaxy syndrome and complete heart block. A 26-year-old healthy female was referred to our clinic in the 23rd week of her pregnancy.
Seçil Kurtulmuş   +4 more
doaj   +2 more sources

Posterior Nutcracker Phenomenon in a Patient with Left Atrial Isomerism

open access: yesThe Thoracic & Cardiovascular Surgeon Reports, 2017
Background Nutcracker phenomenon (NCP) can occur due to various anatomical anomalies. Anterior and posterior NCP are defined in the literature. Posterior NCP combined with left atrial isomerism is a rare condition.
Stanislav Tsvelodub   +3 more
doaj   +2 more sources

Left atrial isomerism associated with aneurysmal enlargement of right atrial appendage: A case report with literature review

open access: yesIndian Journal of Radiology and Imaging, 2019
We present a prenatally diagnosed case of heterotaxy syndrome (HS) in which left atrial isomerism (LAI) was associated with an aneurysmal enlargement of the right atrial appendage (RAA).
Prateek Agarwal, Rajesh Kumar Agarwal
doaj   +2 more sources

Neonatal intra-atrial baffle repair for isolated ventricular inversion with left isomerism: a case report [PDF]

open access: goldSurgical Case Reports, 2020
Background Discordant atrioventricular connection with concordant ventriculoarterial connection, otherwise known as isolated ventricular inversion (IVI), is an extremely rare congenital cardiac malformation.
Yuta Kuwahara   +4 more
doaj   +2 more sources

Ventricular Topology in Congenital Heart Defects Associated with Heterotaxy: Can We Find Patterns Reflecting the Syndrome-Specific Tendency for Visceral Symmetry? [PDF]

open access: yesJournal of Cardiovascular Development and Disease
Heterotaxy syndrome is characterized by a tendency for bilaterally symmetric arrangement (isomerism) of inner organs. It is frequently associated with complex congenital heart defects (CHDs).
Takhfif Othman   +4 more
doaj   +2 more sources

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