PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C0751651|mitochondrial disease |
| Sentences | 5 |
| PubMedID- 24204377 | Furthermore, scn1a alleles have also been recognized to cause autism and epilepsy phenotypes together with biopsy-proven mitochondrial disease (craig et al., 2012). |
| PubMedID- 20668944 | Although these results in pdhc and mitochondrial diseases complicated by epilepsy seem promising, ketogenic diets are often complicated by metabolic disturbances, such as hypoglycemias and hypercholesterolemia as well as by gastrointestinal symptoms and lethargy (duchowny 2005; toshima et al. |
| PubMedID- 23448099 | epilepsy associated with mitochondrial diseases can manifest as infantile spasms; astatic convulsions; myoclonic, focal, or generalized seizures; or as epilepsia partialis continua (canafoglia et al., 2001). |
| PubMedID- 22424762 | We review the effectiveness of the kd in dravet syndrome, epilepsy with myoclonic-atonic seizures, mitochondrial disease, tuberous sclerosis, late infantile and juvenile neuronal ceroid lipofuscinosis, and febrile infection-related epilepsy syndrome. |
| PubMedID- 26381753 | epilepsy in adults with mitochondrial disease: a cohort study. |
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