coexistence of neurofibromatosis type-1 and mthfr c677t gene mutation in a young stroke patient: a case report
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ID: 222720
2013
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Abstract
In neurofibromatosis type-1 (NF1), cerebrovascular disorders are rarely encountered although vasculopathy is a well-known complication. Several mutations seen in methylenetetrahydrofolate reductase (MTHFR) give rise to the formation of hyperhomocysteinemia and homocystinuria, a considerable risk factor for cardiovascular and cerebrovascular disorders, by leading to enzymatic inactivation. In the paper, a 31-year-old young stroke female patient with the coexistence of neurofibromatosis and MTHFR C677T gene mutation was presented.
| Reference Key |
yilmaz2013casecoexistence
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|---|---|
| Authors | ;Halim Yilmaz;Gulten Erkin;Haluk Gumus;Lutfiye Nalbant |
| Journal | journal of pain research |
| Year | 2013 |
| DOI |
10.1155/2013/735419
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| URL | |
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