Results 31 to 40 of about 2,246,280 (273)

A Han-Chinese Fetus With Heterotaxy Syndrome Caused by Novel Compound Heterozygous Mutations in PKD1L1: A Case Report

open access: yesClinical and Experimental Obstetrics & Gynecology
Background: Heterotaxy syndrome is characterized by abnormal organ arrangement across the left-right (L-R) axis, often leading to complex congenital heart defects (CHDs).
Xinyuan Teng   +7 more
doaj   +2 more sources

From multiple spleens to absence: Insights from two cases of heterotaxy syndromes [PDF]

open access: yesRadiology Case Reports
Heterotaxy syndrome is a rare congenital disorder characterized by abnormal arrangement of the thoracic and abdominal organs and is classified into polysplenia (left isomerism) and asplenia (right isomerism) syndromes.
Suman Paudel, MD   +4 more
doaj   +2 more sources

Staged ventricular recruitment following single-ventricular palliation in unbalanced atrioventricular septal defect with heterotaxy syndrome [PDF]

open access: bronzeCardiology in the Young
A newborn with unbalanced atrioventricular septal defect and heterotaxy syndrome underwent early surgeries for single-ventricular palliation due to a small left ventricle.
Somin Im, Jae Gun Kwak, Woong‐Han Kim
openalex   +2 more sources

Heterotaxy polysplenia syndrome with cholangiopancreatic cancer: a case report and literature review

open access: yesFrontiers in Medicine
BackgroundHeterotaxy polysplenia syndrome is a rare condition characterized by multiple abnormal spleens and irregular placement of various organs. Some patients have been documented as developing various types of cancers, although the association with ...
Ziye Chen   +17 more
doaj   +2 more sources

Rare Extracardiac Anomalies Presented with Right Heterotaxy Syndrome in a Newborn Baby: A Case Report. [PDF]

open access: hybridAm J Case Rep, 2020
Huseynova R   +5 more
europepmc   +2 more sources

Dual atrio ventricular node in heterotaxy syndrome [PDF]

open access: yesJournal of Arrhythmia, 2021
Debasis Acharya   +5 more
doaj   +2 more sources

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