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PedAM

Pediatric Disease Annotations & Medicines




Disease mitochondrial disorders
Phenotype C0014544|epilepsy
Sentences 4
PubMedID- 25209085 For those patients with epilepsy due to mitochondrial disorders, lafora disease, unverricht-lundborg disease, and glut1 deficiency syndrome, a successful transition can be even more problematic for both caregivers and neurologists.
PubMedID- 22459315 epilepsy in mitochondrial disorders.
PubMedID- 25440829 Metabolic and mitochondrial disorders associated with epilepsy in children with autism spectrum disorder.
PubMedID- 25606410 Cases reported by the isca consortium with similar deletions, present with epilepsy, another feature of mitochondrial disorders.

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