A Case Report of Marfan Syndrome Presenting With Atypical Chest Pain: A 28-Year-Old Male With Non-ST-Elevation Myocardial Infarction (NSTEMI)

Marfan syndrome is a rare autosomal dominant disorder of the connective tissue. It results in a mutation in the Fibrillin-1 protein gene. We present a case of  Marfan’s syndrome in a young adult with life-threatening, sudden onset of chest pain secondary to a non-ST elevation myocardial infarction (...

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Detalles Bibliográficos
Autores principales: Cheema, Tayyab, Balek, Malek, Smith, Patrick, Hanan, Saad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Cardiac/Thoracic/Vascular Surgery
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916917/
https://www.ncbi.nlm.nih.gov/pubmed/35295345
http://dx.doi.org/10.7759/cureus.22040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916917/
https://www.ncbi.nlm.nih.gov/pubmed/35295345
http://dx.doi.org/10.7759/cureus.22040

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