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- What are mitochondria?
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- General information about mitochondrial disease
- Mitochondrial Reproductive Options
- Specific conditions
- Large-scale mitochondrial DNA deletions
- Neurogenic weakness, Ataxia, and Retinitis Pigmentosa (NARP)
- Multiple mitochondrial DNA deletions
- Mitochondrial Neuro-gastro-intestinal encephalopathy (MNGIE)
- Myoclonic Epilepsy and Ragged Red Fibres (MERRF 8344 A>G)
- Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) 3243 A>G mutation
- Leigh syndrome
- Mitochondrial DNA depletion syndrome (MDDS)
- Alpers’ syndrome
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Patients with mitochondrial disease, along with their families, came together at the Lily family day’s in 2014 and 2015 for a weekend of family fun and interactive seminars. We were very pleased to be part of these fantastic weekends. They provided unique opportunities for patients, clinicians and scientists to interact. Representatives from the Centre highlighted and discussed some of the research happening within the Wellcome Trust Centre for Mitochondrial Research and had direct feedback from patients as a result.
