Mitochondrial respiratory chain diseases are a highly diverse group of diso
rders whose main unifying characteristic is the impairment of mitochondrial
function. As befits an organelle containing gene products encoded by both
mitochondrial DNA (mtDNA) and nuclear DNA (nDNA), these diseases can be cau
sed by inherited errors in either genome, but a surprising number are spora
dic, and a few are even caused by environmental factors.