Compound heterozygosity with methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C mutations likely causing recurrent thrombotic events in a middle-aged man: a case report

Methylenetetrahydrofolate reductase (MTHFR) gene mutations, particularly homozygous mutations, have been associated with a higher incidence of venous thrombosis, coronary heart disease, and obstetric complications. We report the case of a 41-year-old man who presented with multiple vascular thrombot...

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Hauptverfasser:	Yalini Suppu Saravanan, Viswanathan Pandurangan, Devasena Srinivasan
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Ewha Womans University College of Medicine 2026-04-01
Schriftenreihe:	The Ewha Medical Journal
Schlagworte:	compound heterozygosity hyperhomocysteinemia mthfr gene thrombosis case reports
Online-Zugang:	http://www.e-emj.org/upload/pdf/emj-2025-00941.pdf
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