1991Archives of Disease in ChildhoodOpen access

No sensory neuropathy during pyridoxine treatment in homocystinuria.

Chiedzo Mpofu, S M Alani, C. Whitehouse, Brian Fowler, J E Wraith

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Abstract

Seventeen patients with cystathionine synthase deficiency homocystinuria were examined clinically and neurophysiologically for evidence of sensory neuropathy. All had received high dose pyridoxine (vitamin B-6) for many years. Absence of neurological disturbance in all cases suggests long term treatment with pyridoxine in the dosages used in homocystinuric patients is not harmful.

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Seventeen patients with cystathionine synthase deficiency homocystinuria were examined clinically and neurophysiologically for evidence of sensory neuropathy. All had received high dose pyridoxine (vitamin B-6) for many years. Absence of neurological disturbance in all cases suggests long term treatment with pyridoxine in the dosages used in homocystinuric patients is not harmful.

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Available abstract

Seventeen patients with cystathionine synthase deficiency homocystinuria were examined clinically and neurophysiologically for evidence of sensory neuropathy. All had received high dose pyridoxine (vitamin B-6) for many years. Absence of neurological disturbance in all cases suggests long term treatment with pyridoxine in the dosages used in homocystinuric patients is not harmful.

Key concepts: Homocystinuria, Pyridoxine, Medicine, Dose, Vitamin b6, Peripheral neuropathy, Cystathionine beta synthase, Sensory neuropathy

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No sensory neuropathy during pyridoxine treatment in homocystinuria. — Research Paper | ScholarLens