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Gepubliceerd in: Tijdschrift voor Kindergeneeskunde 1/2006

01-02-2006 | Serie wetenschappelijk onderzoek

Stoornissen in de oxidatieve fosforylering: kliniek, diagnostiek en research

Auteurs: M. C. de Vries, E. Morava, M. Hogeveen, R. J. Rodenburg, L. P. W. van den Heuvel, H. J. ter Laak, M. Lammens, L. G. Nijtmans, P. H. Willems, J. A. M. Smeitink

Gepubliceerd in: Tijdschrift voor Kindergeneeskunde | Uitgave 1/2006

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Summary

Oxidative phosphorylation (oxphos) is one of the most important functions of mitochondria, the power plants of the cell. oxphos is the oxidation of substrates and the production of energy as adenosine-triphosphate (atp). Defects of the oxphos-system form a group of diseases that are known as mitochondrial disorders. Most patients develop symptoms in infancy, especially muscle weakness, exercise intolerance and developmental delay. Lactic acid concentration in body fluids does not have to be elevated. Histopathological and especially biochemical investigations of muscle and fibroblasts are an essential part of the diagnostic process. In this report we describe biochemistry, molecular biology, clinical presentation, diagnostics and therapy of oxphos-system defects. The actual research topics of the Nijmegen Center for Mitochondrial Disorders are highlighted, focussing on complex I.
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Metagegevens
Titel
Stoornissen in de oxidatieve fosforylering: kliniek, diagnostiek en research
Auteurs
M. C. de Vries
E. Morava
M. Hogeveen
R. J. Rodenburg
L. P. W. van den Heuvel
H. J. ter Laak
M. Lammens
L. G. Nijtmans
P. H. Willems
J. A. M. Smeitink
Publicatiedatum
01-02-2006
Uitgeverij
Bohn Stafleu van Loghum
Gepubliceerd in
Tijdschrift voor Kindergeneeskunde / Uitgave 1/2006
Print ISSN: 0376-7442
Elektronisch ISSN: 1875-6840
DOI
https://doi.org/10.1007/BF03061596

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