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Mitokondriesygdomme. Klinik, udredning og genetik
Engelsk titel: Mitochondrial diseases. Clinical features, investigation and genetics Läs online Författare: Östergaard E ; Wibrand F ; Horn N ; Bröndum-Nielsen K Språk: Dan Antal referenser: 23 Dokumenttyp: Översikt UI-nummer: 03021098

Tidskrift

Ugeskrift for Laeger 2003;165(7)663-8 ISSN 0041-5782 E-ISSN 1603-6824 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

The aim of this article is to give an overview of mitochondrial disorders. Mitochondria are responsible for the generation of energy in the cells. The term, mitochondrial disorders, usually refers to disorders of the respiratory chain. These disorders can be caused by mutations in the DNA of the mitochondria or in the nuclear DNA. A characteristic feature is that all tissues can be affected, and a defect is expressed differently in different tissues. Highly differentiated energy-demanding tissues, such as neurons and muscle cells, are often affected. Mitochondrial disorders are difficult to diagnose. The investigations comprise metabolic screening, respiratory chain enzyme analysis in muscle tissue, muscle histology, and mutation analysis. The focus of this article is on diagnostic evaluation of childhood disorders, because investigation and diagnosis are particularly difficult in children.