Journal of Inherited Metabolic Disease · 1992 · 154 citations · 11 references
Life SciencesMolecular GeneticsNeurologyMitochondrial BiologyMitochondrial GeneticsMolecular PathologyMitochondrial BiochemistryMitochondrial DiseaseMitochondrial DisordersMitochondrial DysfunctionMitochondrial MetabolismMitochondrial PhysiologyMitochondrial Disease GeneticsMitochondrial Disease PathologyMitochondrial Metabolism DisordersMitochondrial PhenotypingMitochondrial Syndromes
Mitochondrial disorders have long been regarded as neuromuscular diseases only. In fact, owing to the ubiquitous nature of the oxidative phosphorylation, a broad spectrum of clinical features should be expected in mitochondrial disorders. Here, we present eight puzzling observations which give support to the view that a disorder of oxidative phosphorylation can give rise to any symptom in any organ or tissue with any apparent mode of inheritance. Consequently, we suggest giving consideration to the diagnosis of a mitochondrial disorder when dealing with an unexplained association of symptoms, with an early onset and a rapidly progressive course involving seemingly unrelated organs. Determination of lactate/pyruvate and ketone body molar ratios in plasma can help to select patients at risk for this condition.
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Rolf Luft, Denis Ikkos, Genaro M. A. Palmieri et al. · Journal of Clinical Investigation · 1962 · 982 citations · Full text