Category:Leigh syndrome

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<nowiki>sindrome di Leigh; maladie de Leigh; Синдром Лея; Leigh-Syndrom; síndrome de Leigh; بیماری لی; 童年期腦脊髓病變; Leigh hastalığı; 亜急性壊死性脳脊髄障害; Sindrom Leigh; Zespół Leigha; синдром Лея; Syndroom van Leigh; Leigh症候群; متلازمة لي; síndrome de Leigh; Leighin oireyhtymä; Leigh disease; sindromo de Leigh; síndrome de Leigh; Leighov sindrom; malattia della prima infanzia caratterizzata da acidosi lattica, interruzione dello sviluppo psicomotorio, problemi di alimentazione, convulsioni, paralisi extraoculare e debolezza con ipotonia; مرض وراثي; Krankheit; bolezen mitohondrijske presnove, za katero je značilna postopna izguba umskih in gibalnih sposobnosti; simptomi se začnejo med tretjim mesecem in drugim letom starosti in vključujejo izgubo apetita, bruhanje, razdražljivost in epileptične napade; A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.; mitochondrialna choroba metaboliczna; хвороба; Light sendromu mitokondiriyal respiratuvar enzim zincirindeki kusur ve piruvat dehidrogenaz kompleksindeki yetersizlik sonucu beyin beyin sapı omurilikte demyelinazyon gliozis nekros ve kapiller proliferasyonla karakterize bir subakut nekrotizan; Sindrome de Leigh; Enfermedad de Leigh; リー症候群; encéphalopathie nécrosante subaigüe; Encefalopatia necrotizzante subacuta; Malattia di leigh; Choroba Leigha; Лея синдром; Leigh syndroom; Leighsyndroom; Синдром Лейка; Подострая некротизирующая энцефаломиопатия; malaltia de Leigh; encefalomielopatia necrotitzant subaguda; Morbus Leigh; Doença de Leigh; Infantile necrotizing encephalomyelopathy; LEIGH SYNDROME; Leigh's disease (disorder); juvenile subacute necrotizing encephalomyelopathy; subacute necrotizing encephalomyelopathy; Leighin tauti; Leigh综合征; Leighova bolezen; subakutna nekrotizirajoča encefalomielopatija; SNEM</nowiki>
Leigh disease 
A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.
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