Fits, pyridoxine, and hyperprolinaemia type II
Research output: Contribution to journal › Article
The rare inherited disorder hyperprolinaemia type II presents with fits in childhood, usually precipitated by infection. A diagnosis of hyperprolinaemia type II and vitamin B6 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.
|Number of pages||2|
|Journal||Archives of Disease in Childhood|
|Publication status||Published - Mar 2000|