Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
Universidad Médica Pinareña, 2019 Introduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor laterally disorder.
Melissa Toledo Licourt +2 more
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Diffuse hepatocellular carcinoma secondary to cardiac cirrhosis in heterotaxy syndrome. [PDF]
BMJ Case Rep, 2022 Mathavan A +3 more
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Heterotaxy Syndrome with Polysplenism and Left Atrial Isomerism. [PDF]
J Gen Intern Med, 2021 See J, Daingerfield EC, Santos MA.
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Incidental Finding of Heterotaxy Syndrome in a Patient With Pulmonary Embolism: A Case Report and Concise Review. [PDF]
Cureus, 2022 Mahmoud M, El Kortbi K, Wang H, Wang J.
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A Rare Case of Recurrent Pneumonia in Heterotaxy Syndrome, Polysplenia/Left Isomerism. [PDF]
Cureus, 2021 Anwar A, Jubin J, Raza S, Mirza ZK.
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Percutaneous transhepatic access for catheter ablation of a patient with heterotaxy syndrome complicated with atrial fibrillation: A case report. [PDF]
World J Clin Cases, 2022 Wang HX, Li N, An J, Han XB.
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Incidental Heterotaxy Syndrome With Polysplenia and Inferior Vena Cava Agenesis Identified During Trauma Evaluation. [PDF]
CureusAhmed Z +4 more
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Multisystem Phenotypic Spectrum in Pediatric Heterotaxy Syndrome: A Case Series. [PDF]
CureusMukherjee TG +2 more
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Characterization of phenotypic spectrum of fetal heterotaxy syndrome by combining ultrasound and magnetic resonance imaging. [PDF]
Ultrasound Obstet Gynecol, 2021 Seidl-Mlczoch E +9 more
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Heterotaxy syndrome: a rare risk factor for a pulmonary embolism in a young person. [PDF]
Proc (Bayl Univ Med Cent)Mathys L +4 more
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