Conditions

• Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like episodes (MELAS) 3243A>G Mutation
• MERRF (8344A>G Mutation
• Mitochondrial Neuro-Gastro-Intestinal Encephalopathy (MNGIE)
• Single deletions
• Multiple deletions
• Depletion
• Neurogenic Weakness, Ataxia and Retinitis Pigmentosa (NARP)
• Leigh's disease
• Leber's Hereditary Optic Neuropathy (LHON)

 

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