Seizures, Pyridoxine, and Hyperprolinemia Type II

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Type II hyperprolinemia: a case report.

Hyperprolinemia type II (HP II) is a rare inherited metabolic disease due to the deficiency of pyroline-5-carboxylate dehydrogenase. It is generally believed to be a benign condition although some patients have neurological problems such as refractory convulsions. Here we report a six-year-old girl with HP II who admitted to our hospital with recurrent seizure refractory to multiple antiepilept...

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Fits, pyridoxine, and hyperprolinaemia type II.

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ژورنال

عنوان ژورنال: Pediatric Neurology Briefs

سال: 2000

ISSN: 2166-6482,1043-3155

DOI: 10.15844/pedneurbriefs-14-4-4