Fits, pyridoxine, and hyperprolinaemia type II
- PMID: 10685929
- PMCID: PMC1718242
- DOI: 10.1136/adc.82.3.236
Fits, pyridoxine, and hyperprolinaemia type II
Abstract
The rare inherited disorder hyperprolinaemia type II presents with fits in childhood, usually precipitated by infection. A diagnosis of hyperprolinaemia type II and vitamin B(6) deficiency was made in a well nourished child with fits. It is thought that pyridoxine deficiency was implicated in her fits and was the result of inactivation of the vitamin by the proline metabolite, pyrroline-5-carboxylate.
Comment in
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Fits, pyridoxine, and hyperprolinaemia type II.Arch Dis Child. 2000 Jul;83(1):87. doi: 10.1136/adc.83.1.87d. Arch Dis Child. 2000. PMID: 10960335 Free PMC article. No abstract available.
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