Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach
- 1 November 1988
- journal article
- review article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 148 (2) , 92-97
- https://doi.org/10.1007/bf00445910
Abstract
The clinical identification of patients with defects in the mitochondrial respiratory chain is almost impossible. We describe screening tests that should be performed in order to select those patients in whom a skeletal muscle biopsy should be carried out for more specific biochemical assays. The importance of performing in vivo function tests is stressed. The biochemical diagnosis in disorders of the respiratory chain is presented and the application of immunological methods discussed.Keywords
This publication has 19 references indexed in Scilit:
- Mitochondrial myopathiesJournal of Inherited Metabolic Disease, 1987
- Mitochondrial cytopathy with lactic acidosis, carnitine deficiency and DeToni-Fanconi-Debré syndromeBrain & Development, 1986
- Estimation of NADH oxidation in human skeletal muscle mitochondriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1986
- Differential investigation of the capacity of succinate oxidation in human skeletal muscleClinica Chimica Acta; International Journal of Clinical Chemistry, 1985
- Friedreich's ataxiaNeurology, 1984
- A mitochondrial myopathy with a defective respiratory chain and carnitine deficiencyEuropean Journal of Pediatrics, 1983
- Mitochondrial Inheritance in a Mitochondrially Mediated DiseaseNew England Journal of Medicine, 1983
- Pyruvate oxidation in rat and human skeletal muscle mitochondriaBiochemical Medicine, 1978
- Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimensBiochemical Medicine, 1978
- Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal SyndromeScience, 1973