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

Autor: José Fragata, Lídia M Sousa, Fátima F. Pinto, Rui Cerejo, Rui Rodrigues, Carolina Torres, José Diogo Ferreira Martins

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

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 rep

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bfee2033bfdc30fd00d4bfd0b791caa
https://hdl.handle.net/10400.17/3659