Naslov
Cytochrome c Oxidase Partial Deficiency-Associated Leigh Disease Presenting as an Extrapyramidal Syndrome

Autori
Čačić, Melita ; Wilichowski, Ekkehard, Mejaški-Bošnjak, Vlatka ; Fumić, Ksenija ; Lujić, Lucija ; Marušić Della Marina, Branka ; Hanefeld, Folker

Izvornik
Journal of Child Neurology (0883-0738) 16 (2001), 8; 616-619

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Cytochrome c Oxydase; Partial Deficiency; Leigh Disease; Extrapyramidal Syndrome

Sažetak
Leigh disease is a subacute neurodegenerative disorder characterized by simmetric necrotic lesions i the basal ganglia, cerebellum, thalamus, brain stem, and optical nerves and caused by altered oxidative phosphorylation. We dwscribe the clinical, biochemical, neuroimaging, and molecular studies of a 19-year-old boy with early-onset Leigh Disease manifesting as severe extrapyramidal disorder with generalized dystonia and choreoathetosis. He was born of healthy parents after an uneventful pregnancy and delivery. At the age of 2, 5 years, after a minor respiratory infection, he developed unstable, broad-based gait and tremor of the hands. These symptoms persisted for the next several years, when ataxia became more prominent. Difficulty in swallowing, dysarthria, trunk dystonia, and marked dyskinesia of the arms and hands gradually-developed. Nystagmus, transient ptosis, and strabismus alse appeared. Abnormal laboratory findings included elevated plasma and cereblospinal fluid lactate and pyruvate, with an abnormal lactate/pyruvate ratio. Cranial computed tomography and magnetic resonance imaging demonstrated signs of cerebelar atrophy, bilateral and symmetric hypodensities in the lentiform nucleus and thalamus, and transient hyperintensities of cerebral peduncles in T2-weighted sequences suggestive of Leigh disease. Mescle biopsy revealed isolated fiber atrophy, necrotic fibers undergoing phagocytosis, and no ragged-red fibers. The measured catalytic activity of cytochrome c oxidase in skeletal muscle homogenates demonstrated a partial cytochrome c oxidase defficiency. No abnormalities in the mitochondrial genome and in the SURF-1 gene were found. The boy is currently recieving levodopa therapy, creatine monohydrate, and a high dosage of thiamine and lipoic acid, his condition is stabilized, and extrapyramidal symptoms are less pronounced.

Izvorni jezik
Engleski

POVEZANOST RADA