Results 191 to 200 of about 4,489 (232)

A liquid-like organelle at the root of motile ciliopathy [PDF]

open access: yes, 2018
Boulgakov, Alexander A   +7 more
core   +1 more source

Racial disparities in heterotaxy syndrome

Birth Defects Research Part A: Clinical and Molecular Teratology, 2015
BackgroundHeterotaxy syndrome (HTX) is a constellation of defects including abnormal organ lateralization and often including congenital heart defects. HTX has widely divergent population‐based estimates of prevalence, racial and ethnic predominance, and mortality in current literature.MethodsThe objective of this study was to use a population‐based ...
Keila N Lopez   +2 more
exaly   +3 more sources

Echocardiography in Heterotaxy Syndrome

World Journal for Pediatric and Congenital Heart Surgery, 2011
The important anatomic aspects of heterotaxy syndrome can be diagnosed by Doppler echocardiography in the newborn and infant. An organized approach and an understanding of asplenia (right atrial isomerism) and polysplenia (left atrial isomerism) are integral to the echocardiographic study.
openaire   +2 more sources

Intrauterine diagnosis of heterotaxy syndrome

American Heart Journal, 2002
Heterotaxy syndrome, including right isomerism and left isomerism, is characterized by an abnormal symmetry of the viscera and veins and is frequently associated with complex cardiac anomalies. We sought to define the feasibility of in utero diagnosis and the postnatal outcome.Patients with heterotaxy syndrome were identified from 579 fetal ...
Jiuann-Huey, Lin   +7 more
openaire   +2 more sources

Heterotaxy Syndrome with Esophageal Atresia

The Journal of Pediatrics, 2015
newborn presented with a prenatal diagnosis of hy-dramnios, dysplastic kidney, and congenital heart dis-ease and suspected heterotaxy syndrome. His 38-week gestation was complicated by maternal cholestasis. Anamniocentesiswasperformedandkaryotypewas46,XY.Thirdtrimesterserologieswerenegativeandthemotherwasimmuneto rubella and not immune to toxoplasmosis.
Filipa, Flor-de-Lima   +6 more
openaire   +2 more sources

Molecular genetics of heterotaxy syndromes

Current Opinion in Cardiology, 2004
Heterotaxy is a complex set of birth defects in which the normal concordance of asymmetric thoracic and abdominal organs is disturbed. In this review the authors summarize recent research on the etiology of heterotaxy syndromes. Improved understanding of the genetic control of left-right patterning in the early embryo is leading to the identification ...
John W, Belmont   +3 more
openaire   +2 more sources

Fetale Heterotaxie-Syndrome

Der Gynäkologe, 2006
Das mit den Heterotaxie-Syndromen assoziierte Spektrum von Fehlbildungen umfasst eine Vielzahl von kardiovaskularen und viszeralen Anomalien, die mit unterschiedlicher Haufigkeit bei den beiden Hauptvarianten Rechts-Isomerismus und Links-Isomerismus auftreten und sowohl den intrauterinen als auch den postnatalen Verlauf entscheidend beeinflussen. Daher
C. Berg, U. Gembruch, A. Geipel
openaire   +1 more source

Cardiac Rhythm Disturbances in Heterotaxy Syndrome

Pediatric Cardiology, 2019
Heterotaxy syndrome is associated with complex cardiac malformations and cardiac conduction system abnormalities. Those with right atrial isomerism (RAI) have dual sinus nodes and dual atrioventricular nodes predisposing them to supraventricular tachycardia (SVT).
Yui Ozawa   +6 more
openaire   +2 more sources

Diagnosis of heterotaxy syndrome by fetal echocardiography

The American Journal of Cardiology, 1998
We report a series of 13 consecutive patients diagnosed in utero with heterotaxy syndrome in which we found a slight predominance (8 of 13) of fetuses with right atrial isomerism. In previous studies in which diagnosis of left or right isomerism was made based upon findings at fetal echocardiography, there has been a preponderance of infants (95 ...
D E, Atkinson, S, Drant
openaire   +2 more sources

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