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 CASE REPORT
Year : 2020  |  Volume : 30  |  Issue : 5  |  Page : 326-328

Bilateral acute renal infarction secondary to methylene tetrahydrofolate reductase A1298C and PAI-1 mutation


Department of Nephrology, Institute of Renal Science, Sir Gangaram Hospital, New Delhi, India

Correspondence Address:
Dr. Priti Meena
Institute of Renal science, Sir Gangaram Hospital, New Delhi
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijn.IJN_65_20

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We present this rare case of hyperhomocysteinemia due to a mutation in methylene-tetrahydrofolate-reductase (MTFHR) combined with plasminogen activator inhibitor deficiency, causing bilateral renal artery thrombosis. This case highlights the importance of genetic screening in individuals with a family history of thrombotic diseases. There seems to be a role of intervention, even in the setting of renal infarction.






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Indian Journal of Nephrology
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Online since 20th Sept '07