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

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 synd...

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Detalhes bibliográficos
Autor principal: Cerejo, R (author)
Outros Autores: Rodrigues, R (author), Martins, JD (author), Torres, C (author), Sousa, L (author), Pinto, MF (author), Fragata, J (author)
Formato: article
Idioma:eng
Publicado em: 2021
Assuntos:
Adolescent
Coronary Angiography
Coronary Artery Bypass
Electrocardiography
Heart Arrest
Humans
Male
Myocardial Infarction
Progeria
Rare Diseases
HSM CCT
HSM CAR PED
HSM CAR
Texto completo:http://hdl.handle.net/10400.17/3659
País:Portugal
Oai:oai:repositorio.chlc.min-saude.pt:10400.17/3659

Texto Completo

http://hdl.handle.net/10400.17/3659

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