P. Seibel et al., INVESTIGATION ON THE MITOCHONDRIAL TRANSFER RNA(LEU(UUR)) IN BLOOD-CELLS FROM PATIENTS WITH CLUSTER HEADACHE, Journal of neurology, 243(4), 1996, pp. 305-307
Various mutations in the mitochondrial tRNA(Leu(UUR)) gene give rise t
o a variety of neurological disorders. Among these, mitochondrial ence
phalomyopathy, lactic acidosis and stroke-like episodes (MELAS syndrom
e) are frequently associated with a tRNA(Leu(UUR)) mutation at nucleot
ide position 3243 of the mitochondrial DNA. A supplementary clinical f
eature seen in these patients is headache in early life. Recently, a t
RNA(Leu(UUR)) mutation at nucleotide position 3243 has been found in a
patient presenting with cluster headache. This led us to examine the
mitochondrial genomes of 22 patients presenting with cluster headache.
None of the patients harboured the reported tRNA(Leu(UUR)) mutation o
r any other length variations of the mtDNA. Cluster headache is most l
ikely not causally associated with the A3243G mutation of the mitochon
drial DNA.