mitochondrial disease
spontaneously occuring or inherited disorder that involves mitochondrial dysfunction
deafness dystonia syndrome
mitochondrial metabolism disease that is characterized by hearing loss that begins early in life, problems with movement, impaired vision, and behavior problems
Pearson syndrome
mitochondrial metabolism disease
Leigh disease
mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity
GRACILE syndrome
inherited metabolic disease
mitochondrial DNA depletion syndrome
human disease