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Journal of the American Medical Association, 1922
The terms heterotaxy, situs viscerum inversus, lateral inversion of the viscera and, more commonly, transposition of the viscera, are applied to the developmental abnormality in which the viscera normally occupying one side of the body are found on the other.
ELMER H. FUNK, SAMUEL SINGER
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The terms heterotaxy, situs viscerum inversus, lateral inversion of the viscera and, more commonly, transposition of the viscera, are applied to the developmental abnormality in which the viscera normally occupying one side of the body are found on the other.
ELMER H. FUNK, SAMUEL SINGER
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Echocardiography in Heterotaxy Syndrome
World Journal for Pediatric and Congenital Heart Surgery, 2011The 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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Neonatal Assessment of Infants with Heterotaxy
Clinics in Perinatology, 2020Heterotaxy is a generalized term for patients who have an abnormality of laterality that cannot be described as situs inversus. Infants with heterotaxy can have significant anatomic and medical complexity and require personalized, specialized care, including comprehensive anatomic assessment.
Gabrielle C, Geddes +2 more
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Intrauterine diagnosis of heterotaxy syndrome
American Heart Journal, 2002Heterotaxy 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
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Heterotaxy Syndrome with Esophageal Atresia
The Journal of Pediatrics, 2015newborn 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
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Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction
Circulation Genomic and Precision Medicine, 2020Christopher C Y Mak +2 more
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