PT  - JOURNAL ARTICLE
AU  - L Valanne
AU  - L Ketonen
AU  - A Majander
AU  - A Suomalainen
AU  - H Pihko
TI  - Neuroradiologic findings in children with mitochondrial disorders.
DP  - 1998 Feb 01
TA  - American Journal of Neuroradiology
PG  - 369--377
VI  - 19
IP  - 2
4099  - http://www.ajnr.org/content/19/2/369.short
4100  - http://www.ajnr.org/content/19/2/369.full
SO  - Am. J. Neuroradiol.1998 Feb 01; 19
AB  - PURPOSE We report the neuroradiologic findings in 25 children with various mitochondrial diseases.METHODS Twenty-two children with a mitochondrial disorder had MR imaging of the brain and three children had CT studies. In all cases, the diagnosis was based on examination of muscle morphology, analysis of oxygen consumption and respiratory chain enzyme activity in isolated muscle mitochondria, and analysis of rearrangements of the mitochondrial DNA.RESULTS Fifteen patients were found to have the classical syndromes of mitochondrial diseases. Four children had Kearns-Sayre syndrome, but only one had the typical neuroradiologic findings of basal ganglia and brain stem lesions, T2 hyperintensity of the cerebral white matter, and cerebellar atrophy; the others had nonspecific or normal findings. Eight patients had Leigh syndrome, and all showed changes in the putamina. Involvement of the caudate nuclei, globus pallidi, thalami, and brain stem was common, and diffuse supratentorial white matter T2 hyperintensity was seen in two of these patients. Three patients had mitochondrial encephalopathy with lactic acidosis and strokelike episodes (MELAS), with infarctlike lesions that did not correspond to the vascular territories. Ten children with complex I or IV deficiencies and abnormal muscle morphology had nonspecific imaging findings, such as atrophy and abnormal or delayed myelination. One patient with combined complex I and IV deficiency had extensive white matter changes. None of the patients with clinical encephalopathy had normal findings.CONCLUSION MR imaging is helpful in the diagnosis of the classical mitochondrial diseases; however, nonspecific findings are common.