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Chapter 276sTable 1. continuedStudy specifications Patient characteristicsSearch date study numberFirst author Publication yearJournal Publication typeCountries of study Study designNumber of subjects with parkinsonismAge (y) Sex Specific genetic diagnosis70 Marui71 1999 Neuropathology Article Japan case report 1 49 male Down syndrome71 Palat72 2018 Case Rep Neurol Med Article U.S.A. case report 1 20 female Down syndrome72 Singer73 1990 Eur j neurol Article U.S.A. case report 1 45 male Down syndrome73 Storm74 1990 Res dev disabil Article Germany case report 1 21 male Down syndrome74 Sturman75 1989 Lancet Letter U.K. case report 1 23 male Down syndrome75 Camargos76 2008 Lancet neurol Article Brazil case series 4 35 male Dystonia 1675 34 male Dystonia 1675 48 female Dystonia 1675 64 male Dystonia 1676 Keogh77 2014 Neurogenetics Letter U.K. case report 1 12 female Early infantile epileptic encephalopathy 4/ STXBP177 Rezazadeh78 2019 Epilepsy behav Article Canada hidden case 1 46 female Early infantile epileptic encephalopathy 4/STXBP1 78 Yildiz79 2017 Seizure Article Turkey case report 1 13 female Early-onset Lafora disease79 Hall80 2010 Movement disord Article U.S.A. case report 1 61 male Fragile X syndrome80 Rosario81 2018 Movement disord Abstract Portugal case report 1 22 female Hydroxysteroid dehydrogenase type 10 deficiency (HSD10)81 Chen82 2015 Movement disord Abstract U.S.A. case report 1 48 female Incontinentia Pigmenti82 Bach83 2008 Movement Disord Letter Germany case report 1 27 male Klinefelter syndrome83 Lee84 2019 Acta Neurol Belgica Letter Korea case report 1 60 male Klinefelter syndrome84 Yu85 2019 Movement disord Abstract China case report 1 male Klinefelter syndrome85 Fabbri86 2018 Neurol sci Letter Portugal case report 1 37 male Klinefelter syndrome86 Owens87 2004 J neurol neurosur ps Letter U.S.A. case report 1 54 male L2-hydroxyglutaric aciduria87 Martikainen88 2016 JAMA neurol Article U.K. hidden case 1 40 female Leigh syndrome/ mt-ATP688 Baumgartner89 2013 J neurol sci Abstract Austria case report 1 44 male Leigh syndrome/ mt-ATP689 Hemelsoet90 2018 Neurol genet Article Belgium case report 1 44 female Leigh syndrome/mt-FMT90 Martikainen91 2013 Mitochondrion Article Finland case report 1 16 male Leigh-like syndrome91 Zyss92 2011 Movement disord Abstract France case report 1 44 male Mevalonic aciduria92 Alkufri93 2013 Movement disord Article United Kingdomcase report 1 6 female Molybdenum cofactor deficiency type B93 Hara94 2013 Brain dev-jpn Article Japan case report 1 36 male Mucolipidosis type II94 Choi95 2018 Mov disord Article Korea case report 1 54 female Myotonic dystrophy type 195 Pradotto96 2014 Clin neuropathol Abstract Italy case report 1 65 female Neurofibromatosis type 196 Wattanapanom97 2011 J am geriatr soc Abstract U.S.A. hidden case 1 70 male Neurofibromatosis type 197 D’Ambrosio98 1984 Acta neurol Napoli Article Israel case report 1 54 female Neurofibromatosis type 198 Hattori99 1998 Pathol res prac Article Japan case report 1 58 female Neurofibromatosis type 199 Chandra100 2018 Movement Disord Abstract U.S.A. case report 1 33 male NHE6 - Christianson syndrome in males/ SLC9A6100 Pescosolido101 2019 Mol Neuropsychiatry Article U.S.A. other 2 65 female NHE6 - Christianson syndrome in males/ SLC9A6100 55 female NHE6 - Christianson syndrome in males/ SLC9A6