Home›Syndromes affecting the nervous system›síndrome de Karak🌐EspañolEnglishDeutschEspañolFrançaisالعربيةDiseaseQ6368059· pop 8· linked from 4 articlessíndrome de Karakmedical conditionResearch7 papersInfantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis.Brain & development · 2017Loss of PLA2G6 leads to elevated mitochondrial lipid peroxidation and mitochondrial dysfunction.Brain : a journal of neurology · 2015PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.Nature genetics · 2006New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.PloS one · 2013Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum.Journal of medical genetics · 2003via PubMedClinical Trials1 registeredUNKNOWNAvailable in 8 languagesDeutschالعربيةArmenianBanglaPunjabiSerbianWelshvia Wikidata sitelinks · CC0ConnectionsdystoniaEntityJordanCountryCategoriesSyndromes affecting the nervous systemSyndromes with musculoskeletal abnormalities