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Det komplekse kliniske billede ved arvelige mitokondriesygdomme
Engelsk titel: The complex clinical presentation of hereditary mitochondrial diseases Läs online Författare: Frederiksen, Anja Lisbeth ; Frost Nielsen, Morten ; Yderstraede, Knud ; Vissing, John Språk: Dan Antal referenser: 30 Dokumenttyp: Översikt UI-nummer: 14117467

Tidskrift

Ugeskrift for Laeger 2014;176(19)1779-83 ISSN 0041-5782 E-ISSN 1603-6824 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

Mitochondria produce cellular energy, which is of vital importance for cellular metabolism. The organelles contain their own genetic material (i.e. mitochondrial DNA (mtDNA)) with a matrilineal inheritance. Mutations in the mtDNA may cause mitochondrial disease affecting multiple organs leading to diabetes, hearing impairment, muscle fatigue, ptosis and stroke-like episodes in varying combinations and severity. The variable phenotypic presentations make it a challenge to recognize mitochondrial diseases and, consequently, the correct diagnosis is often delayed.