Motor Neuron Syndrome as a New Phenotypic Manifestation of Mutation 9185T>C in Gene MTATP6

Figure 1

Pedigree of family with mitochondriopathy. I-1: death by suicide at 61; I-2: death from haemorragic stroke at 48; II-1: Leigh syndrome, death by suicide at 16 A; II-2: Leigh syndrome, death at 34 A, from respiratory failure; II-3: 34 A, epilepsy, cognitive impairment, and polyneuropathy; II-4: 33 A, index case; II-5: 17 A, cognitive impairment, ataxia, and peripheral neuropathy; II-6: 13 A, neurodevelopmental delay.