Abstract
The plasma levels of urea and ammonia were examined in patients with primary generalized epilepsy, patients with partial epilepsy and in the first-degree relatives of these subjects. The results show a significant decrease in plasma urea in both groups of patients and their first-degree relatives as compared to the non-epileptic controls. The plasma ammonia concentrations were significantly higher in both groups of patients and in the relatives of generalized epilepsy patients as compared to the controls. The observed changes in plasma urea and ammonia were found not to be due to the effect of anticonvulsant drugs. The data suggest that a metabolic defect in urea synthesis may constitute one of the genetic components in the multifactorial etiologies of primary generalized and partial epilepsies.
Original language | English |
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Pages (from-to) | 239-244 |
Number of pages | 6 |
Journal | Epilepsy Research |
Volume | 13 |
Issue number | 3 |
DOIs | |
Publication status | Published - Dec 1992 |
Keywords
- Ammonia
- Metabolic defect, genetic
- Plasma
- Urea
ASJC Scopus subject areas
- Neurology
- Clinical Neurology