Segmental Renal Artery Thrombosis Secondary to Methylene Tetrahydrofolate Reductase Mutation An Unusual Presentation

被引:0
|
作者
Mendonca, Satish [1 ]
Gupta, Devika [2 ]
Gupta, Ankur [3 ]
机构
[1] Pune & Command Hosp, Armed Forces Med Coll, Dept Med, Div Nephrol,So Command, Pune, Maharashtra, India
[2] Pune & Mil Hosp, Armed Forces Med Coll, Dept Pathol, Kirkee, India
[3] Max Superspecial Hosp, Dept Med, Div Nephrol, New Delhi, India
关键词
renal artery thrombosis; methylene tetrahydrofolate reductase gene; hyperhomocysteinemia; VASCULAR-DISEASE; RISK-FACTOR; HYPERHOMOCYSTEINEMIA; GENE;
D O I
暂无
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Methylene tetrahydrofolate reductase (MTHFR) is an enzyme involved in the metabolism of homocysteine to methionine, and folic acid is an essential cofactor. Mutations in the MTHFR gene lead to hyperhomocysteinemia and vascular thrombosis. Heterozygous mutation involving a single nucleotide polymorphism in the MTHFR gene leading to vascular thrombosis is very rare. We present a case of segmental renal artery thrombosis secondary to this mutation and to the best of our knowledge, it is the first case to be reported. Though easily treatable, this is a condition which is seldom investigated in the workup of thrombotic disorders.
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收藏
页码:464 / 466
页数:3
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