Uhl Anomaly

Mazur, Wojciech; Siegel, Marilyn J.; Miszalski−Jamka, Tomasz; Pelberg, Robert

doi:10.1007/978-1-4471-5088-6_8

CT Atlas of Adult Congenital Heart Disease 2013

DOI: 10.1007/978-1-4471-5088-6_8

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Uhl Anomaly

Wojciech Mazur¹,

Marilyn J. Siegel²,

Tomasz Miszalski−Jamka³

et al.

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2018

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Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest

Chounoune

Lowry

Ramakrishnan

et al. 2018

Journal of the Saudi Heart Association

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Uhl's anomaly, first reported in 1952, is an extremely rare congenital cardiac defect characterized by partial or complete loss of the right ventricular myocardium and unknown etiology. Fewer than 100 cases have been described. The response to medical management is poor and there is no known ideal surgical approach or timing for treatment. We report the case of a previously active adolescent male presenting with cardiac arrest, who underwent successful bidirectional cavopulmonary anastomosis ("Glenn" anastomosis) with right atrial reduction and right ventricular free wall plication.

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Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest

Chounoune

Lowry

Ramakrishnan

et al. 2018

Journal of the Saudi Heart Association

View full text Add to dashboard Cite

show abstract

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Uhl Anomaly

Cited by 1 publication

References 5 publications

Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest

Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest

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