Effect of betaine on S ‐adenosylmethionine levels in the cerebrospinal fluid in a patient with methylenetetrahydrofolate reductase deficiency and peripheral neuropathy
- 28 January 1994
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 17 (5) , 560-565
- https://doi.org/10.1007/bf00711591
Abstract
A 16-year-old Japanese girl with 5,10-methylenetetrahydrofolate reductase deficiency showed peripheral neuropathy. There were no significant responses to vitamin B6, vitamin B12 or folate, given alone or in combination. With the addition of betaine monohydrate, she has been free from gait disturbance and muscle weakness. The concentration ofS-adenosylmethionine in cerebrospinal fluid, which was undetectable before receiving betaine monohydrate, increased to about the normal level 24 months after treatment with betaine monohydrate.Keywords
This publication has 17 references indexed in Scilit:
- Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothersAmerican Journal of Medical Genetics, 1993
- Betaine for treatment of homocystinuria caused by methylenetetrahydrofolate reductase deficiency.Archives of Disease in Childhood, 1989
- High-performance liquid chromatographic analysis of fluorescent derivatives of adenine and adenosine and its nucleotidesJournal of Chromatography A, 1989
- Demyelination and decreased S ‐adenosylmethionine in 5.10‐methylenetetrahydrofolate reductase deficiencyNeurology, 1988
- Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolism.Journal of Neurology, Neurosurgery & Psychiatry, 1986
- Central and peripheral nervous system pathology of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiencyPediatric Neurology, 1985
- Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: A case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapyThe Journal of Pediatrics, 1981
- Infantile type of homocystinuria with N5,10-methylenetetrahydrofolate reductase defect.The Tohoku Journal of Experimental Medicine, 1977
- Fluorescent modification of adenosine-containing coenzymes. Biological activities and spectroscopic propertiesBiochemistry, 1972
- Homocystinuria associated with decreased methylenetetrahydrofolate reductase activityBiochemical and Biophysical Research Communications, 1972