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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Splenic Torsion in Heterotaxy Syndrome with Left Isomerism: A Case Report and Literature Review. [PDF]
Diagnostics (Basel), 2022 Cheang IN +4 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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Incidental abdominal heterotaxy syndrome [PDF]
ANZ Journal of Surgery, 2019 Janaka Lovell +2 more
openaire +3 more sources
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.
europepmc +1 more source
Dextrocardia in Heterotaxy Syndrome (Polysplenia Variant) in a 36-Year-Old Ethiopian Woman: A Case Report and Literature Review. [PDF]
Case Rep CardiolTukeni KN +5 more
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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.
europepmc +1 more source
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.
europepmc +1 more source
Incidental Heterotaxy Syndrome With Polysplenia and Inferior Vena Cava Agenesis Identified During Trauma Evaluation. [PDF]
CureusAhmed Z +4 more
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