A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child

Detalhes bibliográficos
Autor(a) principal: Cerejo, R
Data de Publicação: 2020
Outros Autores: Rodrigues, R, Martins, JD, Torres, C, Sousa, L, Pinto, MF, Fragata, J
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/10400.17/3659
Resumo: Hutchinson-Gilford progeria syndrome is a rare genetic disorder, characterized by progressive premature aging and early death in the first or second decade of life, usually secondary to cardiovascular events (myocardial infarction and stroke). We report a case of a 14-year-old boy with progeria syndrome and cardiac arrest due to myocardial infarction, who was submitted to an immediate coronary angiography which revealed left main stem and three-vessel coronary artery disease. A prompt double bypass coronary artery grafting surgery was performed, and, despite successful coronary reperfusion, the patient remained in coma and brain death was declared on fourth day after surgery.
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spelling A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria ChildAdolescentCoronary AngiographyCoronary Artery BypassElectrocardiographyHeart ArrestHumansMaleMyocardial InfarctionProgeriaRare DiseasesHSM CCTHSM CAR PEDHSM CARHutchinson-Gilford progeria syndrome is a rare genetic disorder, characterized by progressive premature aging and early death in the first or second decade of life, usually secondary to cardiovascular events (myocardial infarction and stroke). We report a case of a 14-year-old boy with progeria syndrome and cardiac arrest due to myocardial infarction, who was submitted to an immediate coronary angiography which revealed left main stem and three-vessel coronary artery disease. A prompt double bypass coronary artery grafting surgery was performed, and, despite successful coronary reperfusion, the patient remained in coma and brain death was declared on fourth day after surgery.SAGERepositório da Unidade Local de Saúde São JoséCerejo, RRodrigues, RMartins, JDTorres, CSousa, LPinto, MFFragata, J2021-04-15T14:36:30Z20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/3659eng10.1177/2150135118803596info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-06T16:52:45Zoai:repositorio.chlc.pt:10400.17/3659Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T00:23:35.984239Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
title A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
spellingShingle A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
Cerejo, R
Adolescent
Coronary Angiography
Coronary Artery Bypass
Electrocardiography
Heart Arrest
Humans
Male
Myocardial Infarction
Progeria
Rare Diseases
HSM CCT
HSM CAR PED
HSM CAR
title_short A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
title_full A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
title_fullStr A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
title_full_unstemmed A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
title_sort A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child
author Cerejo, R
author_facet Cerejo, R
Rodrigues, R
Martins, JD
Torres, C
Sousa, L
Pinto, MF
Fragata, J
author_role author
author2 Rodrigues, R
Martins, JD
Torres, C
Sousa, L
Pinto, MF
Fragata, J
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Unidade Local de Saúde São José
dc.contributor.author.fl_str_mv Cerejo, R
Rodrigues, R
Martins, JD
Torres, C
Sousa, L
Pinto, MF
Fragata, J
dc.subject.por.fl_str_mv Adolescent
Coronary Angiography
Coronary Artery Bypass
Electrocardiography
Heart Arrest
Humans
Male
Myocardial Infarction
Progeria
Rare Diseases
HSM CCT
HSM CAR PED
HSM CAR
topic Adolescent
Coronary Angiography
Coronary Artery Bypass
Electrocardiography
Heart Arrest
Humans
Male
Myocardial Infarction
Progeria
Rare Diseases
HSM CCT
HSM CAR PED
HSM CAR
description Hutchinson-Gilford progeria syndrome is a rare genetic disorder, characterized by progressive premature aging and early death in the first or second decade of life, usually secondary to cardiovascular events (myocardial infarction and stroke). We report a case of a 14-year-old boy with progeria syndrome and cardiac arrest due to myocardial infarction, who was submitted to an immediate coronary angiography which revealed left main stem and three-vessel coronary artery disease. A prompt double bypass coronary artery grafting surgery was performed, and, despite successful coronary reperfusion, the patient remained in coma and brain death was declared on fourth day after surgery.
publishDate 2020
dc.date.none.fl_str_mv 2020
2020-01-01T00:00:00Z
2021-04-15T14:36:30Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/3659
url http://hdl.handle.net/10400.17/3659
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1177/2150135118803596
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dc.publisher.none.fl_str_mv SAGE
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instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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