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TÜBİTAK

2019

Mutation

Articles 1 - 1 of 1

Full-Text Articles in Medicine and Health Sciences

The Frequency Of Raynaud?S Phenomenon In Patients With Methylenetetrahydrofolate Reductase Gene Mutation And Hyperhomocysteinemia, Kadi̇r Serkan Yalçin, Ali̇ Koşar Jan 2019

The Frequency Of Raynaud?S Phenomenon In Patients With Methylenetetrahydrofolate Reductase Gene Mutation And Hyperhomocysteinemia, Kadi̇r Serkan Yalçin, Ali̇ Koşar

Turkish Journal of Medical Sciences

Background/aim: Raynaud?s phenomenon (RP) is not a rare health problem; global prevalence is about 3%?20%. Etiology and pathophysiology of this pathology has not been clarified. There are many precipitating factors resulting in RP. Hyperhomocysteinemia resulting from methylenetetrahydrofolate reductase (MTHFR) gene mutationmay have a role in its etiology. The aim of this study was to observe the frequency of RP in patients with MTFHR gene mutation and hyperhomocysteinemia. Possible relationships among vitamin B12, folic acid, complete blood count (leukocytes and platelets), and c-reactive protein levels and RP were also analyzed. Materials and methods: A total of 388 patients admitted to the …