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. 1991 Aug;41(8):1313-5.
doi: 10.1212/wnl.41.8.1313.

Homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency revealed by stroke in adult siblings

J M Visy  1 , P Le Coz, B Chadefaux, C Fressinaud, F Woimant, J Marquet, J Zittoun, J Visy, J M Vallat, M Haguenau
Affiliations

Homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency revealed by stroke in adult siblings

J M Visy et al. Neurology. 1991 Aug.

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.

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  • Homocystinuria.
    Brouwer OF. Brouwer OF. Neurology. 1992 Jun;42(6):1254. doi: 10.1212/wnl.42.6.1254. Neurology. 1992. PMID: 1603359 No abstract available.

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