Acute Coronary Syndrome Treated with Percutaneous Coronary Intervention in Hutchinson–Gilford Progeria

Hutchinson–Gilford progeria syndrome is an extremely rare genetic disease caused by a de novo mutation in the LMNA gene, leading to an accumulation of a form of Lamin A, called Progerin, which results in a typical phenotype and a marked decrease in life expectancy, due to early atherosclerosis and c...

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Detalles Bibliográficos
Autores principales: De Simone, Luciano, Chiellino, Serena, Spaziani, Gaia, Porcedda, Giulio, Calabri, Giovan Battista, Berti, Sergio, Favilli, Silvia, Stefani, Laura, Santoro, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047036/
https://www.ncbi.nlm.nih.gov/pubmed/36980084
http://dx.doi.org/10.3390/children10030526

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047036/
https://www.ncbi.nlm.nih.gov/pubmed/36980084
http://dx.doi.org/10.3390/children10030526

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