Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome

A case of prenatally diagnosed fetal hypertrophic cardiomyopathy is reported. The mother was referred to our department at 37 weeks’ gestation because of suspected congenital heart disease. Prenatal echocardiography showed biventricular hypertrophy and pericardial effusion, without additional abnorm...

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Detalhes bibliográficos
Autores: García Díaz, Lutgardo, Coserria Sánchez, José Félix, Antiñolo Gil, Guillermo
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2012
País:España
Recursos:Universidad de Sevilla (US)
Repositório:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/108021
Acesso em linha:https://hdl.handle.net/11441/108021
https://doi.org/10.1155/2013/472356
Access Level:Acceso aberto
Palavra-chave:Hypertrophic Cardiomyopathy
Prenatal Diagnosis
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spelling Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and OutcomeGarcía Díaz, LutgardoCoserria Sánchez, José FélixAntiñolo Gil, GuillermoHypertrophic CardiomyopathyPrenatal DiagnosisA case of prenatally diagnosed fetal hypertrophic cardiomyopathy is reported. The mother was referred to our department at 37 weeks’ gestation because of suspected congenital heart disease. Prenatal echocardiography showed biventricular hypertrophy and pericardial effusion, without additional abnormalities. Postnatal echocardiography conformed prenatal diagnosis. Neonatal EKG showed biventricular hypertrophy and Wolff-Parkinson-White syndrome. Skeletal muscle biopsy was consistent with mitochondrial oxidative phosphorylation defect involving a combined defect of respiratory complexes I and IV. Echocardiographic followup during the first year of life showed progressive regression of hypertrophy and evolution to left ventricular myocardial noncompactionHindawiCirugía2012info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/108021https://doi.org/10.1155/2013/472356reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésCase Reports in Obstetrics and Gynecology, art.n.472356.https://www.hindawi.com/journals/criog/2013/472356/info:eu-repo/semantics/openAccessoai:idus.us.es:11441/1080212026-06-17T12:51:07Z
dc.title.none.fl_str_mv Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
title Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
spellingShingle Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
García Díaz, Lutgardo
Hypertrophic Cardiomyopathy
Prenatal Diagnosis
title_short Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
title_full Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
title_fullStr Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
title_full_unstemmed Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
title_sort Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome
dc.creator.none.fl_str_mv García Díaz, Lutgardo
Coserria Sánchez, José Félix
Antiñolo Gil, Guillermo
author García Díaz, Lutgardo
author_facet García Díaz, Lutgardo
Coserria Sánchez, José Félix
Antiñolo Gil, Guillermo
author_role author
author2 Coserria Sánchez, José Félix
Antiñolo Gil, Guillermo
author2_role author
author
dc.contributor.none.fl_str_mv Cirugía
dc.subject.none.fl_str_mv Hypertrophic Cardiomyopathy
Prenatal Diagnosis
topic Hypertrophic Cardiomyopathy
Prenatal Diagnosis
description A case of prenatally diagnosed fetal hypertrophic cardiomyopathy is reported. The mother was referred to our department at 37 weeks’ gestation because of suspected congenital heart disease. Prenatal echocardiography showed biventricular hypertrophy and pericardial effusion, without additional abnormalities. Postnatal echocardiography conformed prenatal diagnosis. Neonatal EKG showed biventricular hypertrophy and Wolff-Parkinson-White syndrome. Skeletal muscle biopsy was consistent with mitochondrial oxidative phosphorylation defect involving a combined defect of respiratory complexes I and IV. Echocardiographic followup during the first year of life showed progressive regression of hypertrophy and evolution to left ventricular myocardial noncompaction
publishDate 2012
dc.date.none.fl_str_mv 2012
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/11441/108021
https://doi.org/10.1155/2013/472356
url https://hdl.handle.net/11441/108021
https://doi.org/10.1155/2013/472356
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Case Reports in Obstetrics and Gynecology, art.n.472356.
https://www.hindawi.com/journals/criog/2013/472356/
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Hindawi
publisher.none.fl_str_mv Hindawi
dc.source.none.fl_str_mv reponame:idUS. Depósito de Investigación de la Universidad de Sevilla
instname:Universidad de Sevilla (US)
instname_str Universidad de Sevilla (US)
reponame_str idUS. Depósito de Investigación de la Universidad de Sevilla
collection idUS. Depósito de Investigación de la Universidad de Sevilla
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