Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease epilepsy
Phenotype C0023264|leigh syndrome
Sentences 3
PubMedID- 20332385 A novel presentation of inappropriate antidiuretic hormone secretion in leigh syndrome with the myoclonic epilepsy and ragged red fibers, mitochondrial dna 8344a>g mutation.
PubMedID- 21442960 In 9 children malformations of cns were detected, and in single cases epilepsy was associated with leigh syndrome or nf i, and in one child pituitary microadenoma was detected.
PubMedID- 22981260 Late-onset leigh syndrome with myoclonic epilepsy with ragged-red fibers.

Page: 1