Myotonic Dystrophy-1 Complicated by Factor-V (Leiden) Mutation

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منابع مشابه

Myotonic Dystrophy-1 Complicated by Factor-V (Leiden) Mutation

Objectives. Presence of a factor-V Leiden mutation in a patient with myotonic dystrophy type 1 (DM1) has been reported only once. Here we report the second DM1 patient carrying a factor-V mutation who died from long-term complications of this mutation. Case Report. A 66-year-old DM1 patient with multi-organ-disorder syndrome developed a first deep venous thrombosis (DVT) and consecutive pulmona...

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Myotonic dystrophy complicated by peripheral vascular disease.

Case report A 40-year-old man was admitted to a surgical unit with a 3-week history of increasing pain in the right foot. In the past year he had experienced pain in both calves on walking half a mile, and in addition, had been falling frequently, his legs '6;ving way'. He had had bilateral cataract extractions on,., year previously. There was no history of diabetes melitus or medication. He wa...

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Factor V Leiden mutation in pregnancy.

Normal maternal adaptation to pregnancy significantly increases the risk for thrombus formation. Inherited thrombophilias further increase risk for deep venous thrombosis and adverse outcome in pregnancy. Factor V Leiden mutation is the most common inherited thrombophilia, occurring in approximately 5% of the White and 1% of the Black populations. Nurses should be knowledgeable about screening ...

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Factor V Leiden Mutation Causing Thrombophilia

It has autosomal dominant inheritance and is the most common cause of inherited thrombophilia. FVL is the most prevalent thrombotic risk factor known in the Caucasian population (around 5%). [1] Heterozygotes have a three to five times increased risk of thrombosis. Homozygotes are much less common but have a much higher thrombotic risk, around eight times increased risk. It leads to a hypercoag...

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Factor V Leiden, MTHFR C677T and Prothrombin Gene Mutation G20210A in Iranian Patients with Venous Thrombosis

Background: Factor V Leiden, Prothrombin gene (G20210A) and MTHFR (C677T) polymorphism are the main biomarkers for evaluation of tendency for venous thromboembolism. We aimed to investigate the frequency of mutations in factor V Leiden, Prothrombin G20210A and MTHFR C677T and identify the genetic status for these mutations in patients with venous thrombosis. Methods: This study was carried out...

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ژورنال

عنوان ژورنال: Case Reports in Medicine

سال: 2015

ISSN: 1687-9627,1687-9635

DOI: 10.1155/2015/271639