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Homocystinuria due to 5,10‐methylenetetra‐hydrofolate reductase deficiency revealed by stroke in adult siblings

DOI

85

Citations

0

References

1991

Year

Jean-Marc Visy, P. Le Coz, B. Chadefaux, Catherine Fressinaud, France Woimant, J Marquet, J Zittoun, Jean-Marc Visy, J. M. Vallat, M Haguenau
Neurology

Abstract

Three patients from a single family of six siblings had homocystinemia and homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency and had severe recurrent strokes in adult life. Two of the patients died 1 year after clinical onset.