Results 141 to 150 of about 2,833 (190)

Heterotaxy Syndrome with Asplenia [PDF]

, 2020
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Chronic Cough, Dyspnea, and a Novel CCDC39 Variant: A Case Report of Heterotaxy Syndrome Without Cardiac Anomalies and Associated Primary Ciliary Dyskinesia. [PDF]

Cureus
Juré J, Alexander P.
europepmc   +1 more source

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

Am J Case Rep, 2020
Huseynova R, Bin Mahmoud LA, AlJohani E, Huseynov O, Abdelrahim A, AlOmran KA.   +5 more
europepmc   +1 more source

Heterotaxy Syndrome With Right Isomerism and Interrupted Inferior Vena Cava: A Case Report and Literature Review. [PDF]

Cureus
Iskafi RA, Abugharbieh Y, Ahmad I, Shweki H, Dwaik HA.   +4 more
europepmc   +1 more source

Heterotaxy Syndrome with Polysplenia [PDF]

, 2020
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Fetal Heterotaxy Syndrome [PDF]

Ultrasound in Medicine & Biology, 2017
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Heterotaxy syndrome

, 2015
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Outcomes in adults with congenital heart disease and heterotaxy syndrome: A single-center experience. [PDF]

Congenit Heart Dis, 2019
Broda CR, Salciccioli KB, Lopez KN, Ermis PR, Moodie DS, Dickerson HA.   +5 more
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DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome. [PDF]

Sci Rep, 2019
Liu S, Chen W, Zhan Y, Li S, Ma X, Ma D, Sheng W, Huang G.   +7 more
europepmc   +1 more source

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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.
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