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PedAM

Pediatric Disease Annotations & Medicines




Disease leigh syndrome
Phenotype C0751651|mitochondrial disorder
Sentences 1
PubMedID- 23301511 To investigate the spectrum of common mitochondrial mutations in tunisia during the years of 2002-2012, 226 patients with mitochondrial disorders were clinically diagnosed with hearing loss, leigh syndrome (ls), diabetes, cardiomyopathy, kearns-sayre syndrome (kss), pearson syndrome (ps), myopathy, mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes syndrome (melas) and wolfram syndrome.

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