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Recessive Mitochondrial syndromes: Adult onset CNS Parkinsonism NADH Dehydrogenase, Subunit 1 Alzheimer's/Parkinsonism Leber hereditary optic neuropathy mtRNA Lys (MTTK) : A8344G Parkinson syndrome, Neuropathy & Myopathy 66 mtRNA Thr (MTTT) LHON (G15927A): Variant also described in 1 family with coronary heart disease Occasional sporadic Parkinsonism mtRNA Pro (MTTP) 207 Occasional sporadic Parkinsonism : T15965C mtRNA Pro mutations: Other Myopathy Genetics Mutations may be restricted to muscle C15975T: PEO

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