Journal of Neurology Neurosurgery & Psychiatry · 1993 · 52 citations · 23 references
Mitochondrial MyopathyNeurodegenerative DiseasesMendelian DisorderMitochondrial FunctionShort StatureNeurological DisorderMitochondrial DynamicGenetic DisorderMitochondrial StructurePathologyMitochondrial MedicineMitochondrial BiologyNeurologyMitochondrial EncephalomyopathyDisease Gene IdentificationNeuropathologyMedicineMitochondrial Mutation
The clinical manifestations of mitochondrial encephalomyopathy are described in four generations of a single kindred. The age of onset of major neurological disturbance varied from 3-70 years. In some patients, deafness was the only manifestation; in others, recurrent bouts of status epilepticus associated with focal neurological deficits and headache, caused severe disability or death. Examples of all three adult forms of mitochondrial encephalomyopathy: MELAS, MERFF and Kearns Sayre syndrome, were represented within the kindred. Associated features included deafness, short stature, non-insulin-dependent diabetes mellitus, migraine, peptic ulceration and severe constipation. The nt 3243 A-G MELAS mutation was detected in two members of the kindred. This study highlights the diversity of clinical expression of a mitochondrial mutation within a single kindred.
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A Direct Repeat Is a Hotspot for Large-Scale Deletion of Human Mitochondrial DNA
Eric A. Schon, Rosario Rizzuto, Carlos T. Moraes et al. · Science · 1989 · 579 citations
Kearns-sayre Syndrome, Dna, Genetics +23