5C53.24Ангилал

Leigh syndrome

Тодорхойлолт

Leigh syndrome or subacute necrotizing encephalomyelopathy is a progressive neurological disease defined by specific neuropathological features associating brainstem and basal ganglia lesions. Loss of motor milestones, hypotonia with poor head control, recurrent vomiting, and a movement disorder are common initial symptoms. Pyramidal and extrapyramidal signs, nystagmus, breathing disorders, ophthalmoplegia and peripheral neuropathy are often noted later. Epilepsy is relatively uncommon. Leigh syndrome has multiple causes, all of which imply a defect in aerobic energy production, ranging from the pyruvate dehydrogenase complex to the oxidative phosphorylation pathway.

Индексийн нэр томьёо Index terms · 22

Leigh syndromeLeigh diseaseInfantile subacute necrotizing encephalopathysubacute necrotising encephalomyelopathySubacute necrotising encephalopathyLeigh syndrome due to cytochrome C oxidase deficiencyLeigh syndrome with cardiomyopathyCardiomyopathy - hypotonia, due to cytochrome C oxidase deficiencyCardiomyopathy with myopathy due to COX deficiencyLeigh syndrome with leukodystrophyInfantile subacute necrotizing encephalopathy with leukodystrophyLeigh syndrome with nephrotic syndromeSaguenay-Lac-Saint-Jean cytochrome C oxidase deficiencyFrench-Canadian cytochrome C oxidase deficiencyLeigh syndrome, Saguenay-Lac-St. Jean typeLeigh syndrome, French-Canadian typeCOX deficiency, French-Canadian typeSLSJ-COX - [Saguenay-Lac-Saint-Jean cytochrome C oxidase] deficiencyDystonia due to Leigh syndromeDystonia due to subacute necrotizing encephalomyelopathySporadic Leigh syndromeSporadic infantile subacute necrotizing encephalopathy

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