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

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 s...

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Autores principales: Chounoune, Reginald, Lowry, Adam, Ramakrishnan, Karthik, Pearson, Gail D., Moak, Jeffrey P., Nath, Dilip S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744023/
https://www.ncbi.nlm.nih.gov/pubmed/29296065
http://dx.doi.org/10.1016/j.jsha.2017.03.011
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author Chounoune, Reginald
Lowry, Adam
Ramakrishnan, Karthik
Pearson, Gail D.
Moak, Jeffrey P.
Nath, Dilip S.
author_facet Chounoune, Reginald
Lowry, Adam
Ramakrishnan, Karthik
Pearson, Gail D.
Moak, Jeffrey P.
Nath, Dilip S.
author_sort Chounoune, Reginald
collection PubMed
description 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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spelling pubmed-57440232018-01-02 Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest Chounoune, Reginald Lowry, Adam Ramakrishnan, Karthik Pearson, Gail D. Moak, Jeffrey P. Nath, Dilip S. J Saudi Heart Assoc Case Report 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. Elsevier 2018-01 2017-04-07 /pmc/articles/PMC5744023/ /pubmed/29296065 http://dx.doi.org/10.1016/j.jsha.2017.03.011 Text en © 2017 King Saud University http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Chounoune, Reginald
Lowry, Adam
Ramakrishnan, Karthik
Pearson, Gail D.
Moak, Jeffrey P.
Nath, Dilip S.
Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest
title Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest
title_full Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest
title_fullStr Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest
title_full_unstemmed Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest
title_short Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest
title_sort uhl’s anomaly: a one and a half ventricular repair in a patient presenting with cardiac arrest
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744023/
https://www.ncbi.nlm.nih.gov/pubmed/29296065
http://dx.doi.org/10.1016/j.jsha.2017.03.011
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