Results 31 to 40 of about 1,224,037 (184)

Respiratory complications in patients with heterotaxy syndrome.

open access: yes, 2012
Respiratory complications in patients with heterotaxy ...
P. Versacci, V. Martucci, D. Marino
core   +1 more source

Heterotaxy syndrome: Prenatal diagnosis, concomitant malformations and outcomes

open access: yes, 2022
Objective The aim of this study is to define cardiac and extracardiac malformations in fetuses with heterotaxy syndrome and to determine perinatal and childhood prognosis. Methods In this retrospective study, fetuses diagnosed with heterotaxy syndrome on
Demirci, Oya   +3 more
core   +1 more source

Aortic pseudocoarctation associated with polysplenia/heterotaxy syndrome

open access: yesRevista Portuguesa de Cardiologia, 2015
Polysplenia/heterotaxy syndrome is a rare congenital disorder associated with a wide spectrum of anomalies in various organ systems. Although anomalies of the cardiovascular system are common in this syndrome, the authors report a rare case of ...
Ricardo Duarte, Humberto Morais
doaj   +1 more source

A rare case of heterotaxy and left ventricular non-compaction in an adult [PDF]

open access: yes, 2016
Heterotaxy syndrome with left ventricular non-compaction is a rare co-existence of abnormalities with unknown cause. It can be isolated with no other associations, or associated with congenital heart diseases, or it can occur with multiple other ...
Chacko, Anith   +3 more
core   +1 more source

Novel use of covered stents to treat profound cyanosis in a hepatic vein exclusion Fontan

open access: yesAnnals of Pediatric Cardiology, 2019
Fontan completion in patients with complex cardiac anatomy, and specifically heterotaxy syndrome, can present unique physiologic considerations. For example, existing venous connections may be “unmasked” after a cavopulmonary anastomosis operation.
Sarosh P Batlivala, Makram R Ebeid
doaj   +1 more source

Polysplenia syndrome with complex heart disease and jejunal atresia with malrotation in neonate: A case report

open access: yesClinical Case Reports, 2020
Polysplenia is heterotaxy syndrome or bilateral left‐sidedness. We report a case of polysplenia syndrome in order to draw attention to this rare syndrome that must be excluded in an infant presenting with congenital heart disease and intestinal ...
Roya Arif Huseynova   +4 more
doaj   +1 more source

Management for Heterotaxy Syndrome With Functional Single Ventricle and Extracardiac Total Anomalous Pulmonary Venous Connection

open access: yesTokyo Women's Medical University Journal, 2023
Background: Heterotaxy syndrome associated with functional single ventricle and extracardiac total anomalous pulmonary venous connection (TAPVC) is characterized by high operative risks and has high mortality rate.
Minori Tateishi, Masaaki Koide
doaj   +1 more source

Noncompaction cardiomyopathy and heterotaxy syndrome. [PDF]

open access: yesProg Pediatr Cardiol, 2017
Left ventricular noncompaction cardiomyopathy (LVNC) is characterized by compact and trabecular layers of the left ventricular myocardium. This cardiomyopathy may occur with congenital heart disease (CHD).
Martinez HR   +3 more
europepmc   +2 more sources

Prenatal Findings in Left Atrial Isomerism and an Overview of Heterotaxy Syndrome

open access: yes, 2017
Heterotaxy syndrome is a rare, complex disorder involving structural cardiac defects in combination with symmetrical development of abdominal viscera that are normally asymmetrical organs.
Samantha N. Sawyer, Claudine Thomas
core   +1 more source

Small RNA pathways in mammalian oocytes

open access: yesFEBS Open Bio, EarlyView.
Three distinct small RNA pathways operate in mammalian oocytes: RNAi interference (RNAi), the microRNA (miRNA) pathway, and the PIWI‐associated RNA (piRNA) pathway. These pathways use small RNAs to guide sequence‐specific repression and contribute to oocyte biology by targeting genes and mobile elements or appear insignificant since different ...
Petr Svoboda, Josef Pasulka
wiley   +1 more source

Home - About - Disclaimer - Privacy