Skip to main content

Parkinson’s Disease

  • Chapter
  • First Online:
Neurological Disorders in the Arab World

Abstract

Parkinson’s disease (PD) is a common neurodegenerative disorder. As it affects particularly the elderly, it is expected to contribute to the economic and social burden on populations as they age. This chapter discusses the epidemiological and genetic data related to PD in Arabs. The PD incidence rates reported from Libya and Egypt lie outside the range of rates reported elsewhere: the incidence in Libya is below the range while in Egypt it is above it. Most of the Libyan population is young, which could explain the low incidence of PD, but the Egyptian findings are difficult to explain. The prevalence data from the Arab countries show the same pattern as the incidence data. The majority of the prevalence rates are low, while one Egyptian study shows an exceptionally high prevalence. Four chromosomal loci (PARK2, PARK6, PARK8, and PARK9) associated with the causative genes (Parkin, PINK1, LRRK2 and ATP132A) have been reported in Arabs. All the genes described in Arabs are inherited as autosomal recessive, except for LRRK2, which is inherited as autosomal dominant. The frequency of LRRK2 G2019S is uniquely high at 30−42 % in familial PD and 30−39 % in apparently sporadic PD in Maghreb (North African) populations. This frequency is the highest reported anywhere in the world so far. The implication of that is not fully understood. There is only one study from Arab countries outside Maghreb populations. An Egyptian study found a frequency rate of 10 % of LRRK2 G2019S in apparently sporadic PD. Although methodological issues and population age structures could partially explain the incidence and prevalence of PD in Libya and Egypt, further studies are needed. Also, additional investigation of LRRK2 G2019S in Arab countries is needed.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 59.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 79.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 109.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Parkinson J. An essay on the Shaking Palsy. Dr. Jordi Segarra (DU PONT Pharma): London; 1817.

    Google Scholar 

  2. Mutch WJ, Dingwall-Fordyce I, Downie AW, Paterson JG, Roy SK. Parkinson’s disease in a Scottish city. Br Med J (Clin Res Ed). 1986;292(6519):534–6.

    Article  CAS  Google Scholar 

  3. de Lau LM, Breteler MM. Epidemiology of Parkinson’s disease. Lancet Neurol. 2006;5(6):525–35.

    Article  PubMed  Google Scholar 

  4. Dorsey ER, Constantinescu R, Thompson JP, Biglan KM, Holloway RG, Kieburtz K, et al. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology. 2007;68(5):384–6.

    Article  CAS  PubMed  Google Scholar 

  5. Al-Rajeh S, Awada A, Bademosi O, Ismail H. Spectrum of movement disorders in a Saudi University Hospital. Saudi Med J. 1994;15(2):138–42.

    Google Scholar 

  6. Glik A, Masarwa M, Abuful A, Deeb A, Strugatsky R, Farrer LA, et al. Essential tremor might be less frequent than Parkinson’s disease in North Israel Arab villages. Mov Disord. 2009;24(1):119–22.

    Article  PubMed Central  PubMed  Google Scholar 

  7. Mizuno Y, Hattori N, Mochizuki H. Etiology of Parkinson’s disease. In: Watts RL, Koller WC, editors. Movement disorders: neurologic principles & practice. New York: McGraw-Hill; 2004. p. 209–31.

    Google Scholar 

  8. Gibb WR, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson’s disease. J Neurol Neurosurg Psychiatry. 1988;51(6):745–52.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  9. Van Den Eeden SK, Tanner CM, Bernstein AL, Fross RD, Leimpeter A, Bloch DA, et al. Incidence of Parkinson’s disease: variation by age, gender, and race/ethnicity. Am J Epidemiol. 2003;157(11):1015–22.

    Article  Google Scholar 

  10. Ashok PP, Radhakrishnan K, Sridharan R, Mousa ME. Epidemiology of Parkinson’s disease in Benghazi, North-East Libya. Clin Neurol Neurosurg. 1986;88(2):109–13.

    Article  CAS  PubMed  Google Scholar 

  11. Khedr EM, Al Attar GS, Kandil MR, Kamel NF, Abo Elfetoh N, Ahmed MA. Epidemiological study and clinical profile of Parkinson’s disease in the Assiut Governorate, Egypt: a community-based study. Neuroepidemiology. 2012;38(3):154–63.

    Article  PubMed  Google Scholar 

  12. Granieri E, Carreras M, Casetta I, Govoni V, Tola MR, Paolino E, et al. Parkinson’s disease in Ferrara, Italy, 1967 through 1987. Arch Neurol. 1991;48(8):854–7.

    Article  CAS  PubMed  Google Scholar 

  13. Fall PA, Axelson O, Fredriksson M, Hansson G, Lindvall B, Olsson JE, et al. Age-standardized incidence and prevalence of Parkinson’s disease in a Swedish community. J Clin Epidemiol. 1996;49(6):637–41.

    Article  CAS  PubMed  Google Scholar 

  14. MacDonald BK, Cockerell OC, Sander JW, Shorvon SD. The incidence and lifetime prevalence of neurological disorders in a prospective community-based study in the UK. Brain. 2000;123(Pt 4):665–76.

    Article  PubMed  Google Scholar 

  15. Kusumi M, Nakashima K, Harada H, Nakayama H, Takahashi K. Epidemiology of Parkinson’s disease in Yonago City, Japan: comparison with a study carried out 12 years ago. Neuroepidemiology. 1996;15(4):201–7.

    Article  CAS  PubMed  Google Scholar 

  16. Harada H, Nishikawa S, Takahashi K. Epidemiology of Parkinson’s disease in a Japanese city. Arch Neurol. 1983;40(3):151–4.

    Article  CAS  PubMed  Google Scholar 

  17. Twelves D, Perkins KS, Counsell C. Systematic review of incidence studies of Parkinson’s disease. Mov Disord. 2003;18(1):19–31.

    Article  PubMed  Google Scholar 

  18. Sutcliffe RL, Meara JR. Parkinson’s disease epidemiology in the Northampton District, England, 1992. Acta Neurol Scand. 1995;92(6):443–50.

    Article  CAS  PubMed  Google Scholar 

  19. Mayeux R, Marder K, Cote LJ, Denaro J, Hemenegildo N, Mejia H, et al. The frequency of idiopathic Parkinson’s disease by age, ethnic group, and sex in northern Manhattan, 1988–1993. Am J Epidemiol. 1995;142(8):820–7.

    CAS  PubMed  Google Scholar 

  20. Marras C, Tanner CM. Epidemiology of Parkinson’s disease. In: Watts RL, Koller WC, editors. Movement disorders: neurologic principles & practice. New York: McGraw-Hill; 2004. p. 177–95.

    Google Scholar 

  21. El Tallawy HN, Farghaly WM, Rageh TA, Shehata GA, Metwaly NA, Elftoh NA, et al. Epidemiology of major neurological disorders project in Al Kharga District, New Valley, Egypt. Neuroepidemiology. 2010;35(4):291–7.

    Article  PubMed  Google Scholar 

  22. El Tallawy HN, Farghaly WM, Rageh TA, Shehata GA, Badry R, Metwally NA, et al. Door-to-door survey of major neurological disorders (project) in Al Quseir City, Red Sea Governorate, Egypt. Neuropsychiatr Dis Treat. 2013;9:767–71.

    PubMed Central  PubMed  Google Scholar 

  23. Al-Rajeh S, Bademosi O, Ismail H, Awada A, Dawodu A, Al-Freihi H, et al. A community survey of neurological disorders in Saudi Arabia: the Thugbah study. Neuroepidemiology. 1993;12(3):164–78.

    Article  CAS  PubMed  Google Scholar 

  24. Attia Romdhane N, Ben Hamida M, Mrabet A, Larnaout A, Samoud S, Ben Hamda A, et al. Prevalence study of neurologic disorders in Kelibia (Tunisia). Neuroepidemiology. 1993;12(5):285–99.

    Article  CAS  PubMed  Google Scholar 

  25. Alrefai A, Habahbih M, Alkhawajah M, Darwish M, Batayha W, Khader Y, et al. Prevalence of Parkinson’s disease in Northern Jordan. Clin Neurol Neurosurg. 2009;111(10):812–5.

    Article  PubMed  Google Scholar 

  26. Masalha R, Kordysh E, Alpert G, Hallak M, Morad M, Mahajnah M, et al. The prevalence of Parkinson’s disease in an Arab population, Wadi Ara, Israel. Isr Med Assoc J. 2010;12(1):32–5.

    PubMed  Google Scholar 

  27. Osuntokun BO, Adeuja AO, Schoenberg BS, Bademosi O, Nottidge VA, Olumide AO, et al. Neurological disorders in Nigerian Africans: a community-based study. Acta Neurol Scand. 1987;75(1):13–21.

    Article  CAS  PubMed  Google Scholar 

  28. Tekle-Haimanot R, Abebe M, Gebre-Mariam A, Forsgren L, Heijbel J, Holmgren G, et al. Community-based study of neurological disorders in rural central Ethiopia. Neuroepidemiology. 1990;9(5):263–77.

    Article  CAS  PubMed  Google Scholar 

  29. Okubadejo NU, Bower JH, Rocca WA, Maraganore DM. Parkinson’s disease in Africa: a systematic review of epidemiologic and genetic studies. Mov Disord. 2006;21(12):2150–6.

    Article  PubMed  Google Scholar 

  30. Wickremaratchi MM, Perera D, O’Loghlen C, Sastry D, Morgan E, Jones A, et al. Prevalence and age of onset of Parkinson’s disease in Cardiff: a community based cross sectional study and meta-analysis. J Neurol Neurosurg Psychiatry. 2009;80(7):805–7.

    Article  CAS  PubMed  Google Scholar 

  31. von Campenhausen S, Bornschein B, Wick R, Bötzel K, Sampaio C, Poewe W, et al. Prevalence and incidence of Parkinson’s disease in Europe. Eur Neuropsychopharmacol. 2005;15(4):473–90.

    Article  Google Scholar 

  32. Bhidayasiri R, Wannachai N, Limpabandhu S, Choeytim S, Suchonwanich Y, Tananyakul S, et al. A national registry to determine the distribution and prevalence of Parkinson’s disease in Thailand: implications of urbanization and pesticides as risk factors for Parkinson’s disease. Neuroepidemiology. 2011;37(3–4):222–30.

    Article  PubMed  Google Scholar 

  33. Bharucha NE, Bharucha EP, Bharucha AE, Bhise AV, Schoenberg BS. Prevalence of Parkinson’s disease in the Parsi community of Bombay, India. Arch Neurol. 1988;45(12):1321–3.

    Article  CAS  PubMed  Google Scholar 

  34. Mayeux R, Denaro J, Hemenegildo N, Marder K, Tang MX, Cote LJ, et al. A population-based investigation of Parkinson’s disease with and without dementia. Relationship to age and gender. Arch Neurol. 1992;49(5):492–7.

    Article  CAS  PubMed  Google Scholar 

  35. Caradoc-Davies TH, Weatherall M, Dixon GS, Caradoc-Davies G, Hantz P. Is the prevalence of Parkinson’s disease in New Zealand really changing? Acta Neurol Scand. 1992;86(1):40–4.

    Article  CAS  PubMed  Google Scholar 

  36. Chen RC, Chang SF, Su CL, Chen TH, Yen MF, Wu HM, et al. Prevalence, incidence, and mortality of PD: a door-to-door survey in Ilan county, Taiwan. Neurology. 2001;57(9):1679–86.

    Article  CAS  PubMed  Google Scholar 

  37. Rosati G, Granieri E, Pinna L, Aiello I, Tola R, De BP, et al. The risk of Parkinson disease in Mediterranean people. Neurology. 1980;30(3):250–5.

    Article  CAS  PubMed  Google Scholar 

  38. Wermuth L, von Weitzel-Mudersbach P, Jeune B. A two-fold difference in the age-adjusted prevalences of Parkinson’s disease between the island of Als and the Faroe Islands. Eur J Neurol. 2000;7(6):655–60.

    Article  CAS  PubMed  Google Scholar 

  39. Newman EJ, Grosset KA, Grosset DG. Geographical difference in Parkinson’s disease prevalence within West Scotland. Mov Disord. 2009;24(3):401–6.

    Article  PubMed  Google Scholar 

  40. Wooten GF, Currie LJ, Bovbjerg VE, Lee JK, Patrie J. Are men at greater risk for Parkinson’s disease than women? J Neurol Neurosurg Psychiatry. 2004;75(4):637–9.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  41. Dick FD. Parkinson’s disease and pesticide exposures. Br Med Bull. 2006;79–80:219–31.

    Article  PubMed  Google Scholar 

  42. Dick FD, De Palma G, Ahmadi A, Scott NW, Prescott GJ, Bennett J, et al. Environmental risk factors for Parkinson’s disease and parkinsonism: the Geoparkinson study. Occup Environ Med. 2007;64(10):666–72.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  43. Tüchsen F, Jensen AA. Agricultural work and the risk of Parkinson’s disease in Denmark, 1981–1993. Scand J Work Environ Health. 2000;26(4):359–62.

    Article  PubMed  Google Scholar 

  44. Gorell JM, Johnson CC, Rybicki BA, Peterson EL, Richardson RJ. The risk of Parkinson’s disease with exposure to pesticides, farming, well water, and rural living. Neurology. 1998;50(5):1346–50.

    Article  CAS  PubMed  Google Scholar 

  45. Bronstein J, Carvey P, Chen H, Cory-Slechta D, DiMonte D, Duda J, et al. Meeting report: consensus statement-Parkinson’s disease and the environment: collaborative on health and the environment and Parkinson’s Action Network (CHE PAN) conference 26–28 June 2007. Environ Health Perspect. 2009;117(1):117–21.

    Article  PubMed Central  PubMed  Google Scholar 

  46. Thomas B, Beal MF. Parkinson’s disease. Hum Mol Genet. 2007; 16 Spec No. 2:R183–194.

    Google Scholar 

  47. Klein C, Westenberger A. Genetics of Parkinson’s disease. Cold Spring Harb Perspect Med. 2012;2:a008888.

    Article  PubMed Central  PubMed  Google Scholar 

  48. Gouider-Khouja N, Belal S, Hamida MB, Hentati F. Clinical and genetic study of familial Parkinson’s disease in Tunisia. Neurology. 2000;54(8):1603–9.

    Article  CAS  PubMed  Google Scholar 

  49. Gasser T. Genetics of Parkinson’s disease. Curr Opin Neurol. 2005;18(4):363–9.

    Article  CAS  PubMed  Google Scholar 

  50. Lewthwaite AJ, Nicholl DJ. Genetics of parkinsonism. Curr Neurol Neurosci Rep. 2005;5(5):397–404.

    Article  CAS  PubMed  Google Scholar 

  51. Houlden H, Singleton AB. The genetics and neuropathology of Parkinson’s disease. Acta Neuropathol. 2012;124(3):325–38.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  52. Saiki S, Sato S, Hattori N. Molecular pathogenesis of Parkinson’s disease: update. J Neurol Neurosurg Psychiatry. 2012;83(4):430–6.

    Article  PubMed  Google Scholar 

  53. Lucking CB, Abbas N, Durr A, Bonifati V, Bonnet AM, de Broucker T, et al. Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson’s Disease and the French Parkinson’s Disease Genetics Study Group. Lancet. 1998;352(9137):1355–6.

    Article  CAS  PubMed  Google Scholar 

  54. Tassin J, Durr A, de Broucker T, Abbas N, Bonifati V, De Michele G, et al. Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson’s Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson’s Disease. Am J Hum Genet. 1998;63(1):88–94.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  55. Myhre R, Steinkjer S, Stormyr A, Nilsen GL, Abu ZH, Horany K, et al. Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism. BMC Neurol. 2008;8:47.

    Article  PubMed Central  PubMed  Google Scholar 

  56. Jones AC, Yamamura Y, Almasy L, Bohlega S, Elibol B, Hubble J, et al. Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region. Am J Hum Genet. 1998;63(1):80–7.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  57. Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, et al. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study. Parkinsonism Relat Disord. 2003;9(5):247–51.

    Article  PubMed  Google Scholar 

  58. Nisipeanu P, Inzelberg R, Abo Mouch S, Carasso RL, Blumen SC, Zhang J, et al. Parkin gene causing benign autosomal recessive juvenile parkinsonism. Neurology. 2001;56(11):1573–5.

    Article  CAS  PubMed  Google Scholar 

  59. Valente EM, Bou-Sleiman PM, Caputo V, Muqit MM, Harvey K, Gispert S, et al. Hereditary early-onset Parkinson’s disease caused by mutations in PINK1. Science. 2004;304(5674):1158–60.

    Article  CAS  PubMed  Google Scholar 

  60. Valente EM, Salvi S, Ialongo T, Marongiu R, Elia AE, Caputo V, et al. PINK1 mutations are associated with sporadic early-onset parkinsonism. Ann Neurol. 2004;56(3):336–41.

    Article  CAS  PubMed  Google Scholar 

  61. Ibanez P, Lesage S, Lohmann E, Thobois S, De Michele G, Borg M, et al. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain. 2006;129(Pt 3):686–94.

    Article  PubMed  Google Scholar 

  62. Chishti MA, Bohlega S, Ahmed M, Loualich A, Carroll P, Sato C, et al. T313M PINK1 mutation in an extended highly consanguineous Saudi family with early-onset Parkinson disease. Arch Neurol. 2006;63(10):1483–5.

    Article  PubMed  Google Scholar 

  63. Leutenegger AL, Salih MA, Ibanez P, Mukhtar MM, Lesage S, Arabi A, et al. Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1. Arch Neurol. 2006;63(9):1257–61.

    Article  PubMed  Google Scholar 

  64. Cazeneuve C, San C, Ibrahim SA, Mukhtar MM, Kheir MM, LeGuern E, et al. A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson’s disease. Neurogenetics. 2009;10(3):265–70.

    Article  CAS  PubMed  Google Scholar 

  65. Ishihara-Paul L, Hulihan MM, Kachergus J, Upmanyu R, Warren L, Amouri R, et al. PINK1 mutations and parkinsonism. Neurology. 2008;71(12):896–902.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  66. Healy DG, Falchi M, O’Sullivan SS, Bonifati V, Durr A, Bressman S, et al. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson’s disease: a case–control study. Lancet Neurol. 2008;7(7):583–90.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  67. Lesage S, Belarbi S, Troiano A, Condroyer C, Hecham N, Pollak P, et al. Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease? Neurology. 2008;71(19):1550–2.

    Article  CAS  PubMed  Google Scholar 

  68. Nishioka KMP, Kefi MM, Jasinska-Myga BMP, Wider CM, Vilarino-Guell CP, Ross OAP, et al. A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson disease. J Neurol Neurosurg Psychiatry. 2010;81(4):391–95.

    Article  PubMed  Google Scholar 

  69. Hashad DI, Abou-Zeid AA, Achmawy GA, Allah HM, Saad MA. G2019S mutation of the leucine-rich repeat kinase 2 gene in a cohort of Egyptian patients with Parkinson’s disease. Genet Test Mol Biomarkers. 2011;15(12):861–6.

    Article  CAS  PubMed  Google Scholar 

  70. Belarbi S, Hecham N, Lesage S, Kediha MI, Smail N, Benhassine T, et al. LRRK2 G2019S mutation in Parkinson’s disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort. Parkinsonism Relat Disord. 2010;16(10):676–9.

    Article  PubMed  Google Scholar 

  71. Ben Sassi S, Nabli F, Hentati E, Nahdi H, Trabelsi M, Ben Ayed H, et al. Cognitive dysfunction in Tunisian LRRK2 associated Parkinson’s disease. Parkinsonism Relat Disord. 2012;18(3):243–6.

    Article  PubMed  Google Scholar 

  72. Brett M, Fentress EWB. The Berbers. Oxford: Blackwell; 1997.

    Google Scholar 

  73. Lesage S, Durr A, Tazir M, Lohmann E, Leutenegger AL, Janin S, et al. LRRK2 G2019S as a cause of Parkinson’s disease in North African Arabs. N Engl J Med. 2006;354(4):422–3.

    Article  CAS  PubMed  Google Scholar 

  74. Lesage S, Ibanez P, Lohmann E, Pollak P, Tison F, Tazir M, et al. G2019S LRRK2 mutation in French and North African families with Parkinson’s disease. Ann Neurol. 2005;58(5):784–7.

    Article  CAS  PubMed  Google Scholar 

  75. Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, et al. Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson’s disease families. Mov Disord. 2007;22(1):55–61.

    Article  PubMed  Google Scholar 

  76. Hulihan MM, Ishihara-Paul L, Kachergus J, Warren L, Amouri R, Elango R, et al. LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case–control genetic study. Lancet Neurol. 2008;7(7):591–4.

    Article  CAS  PubMed  Google Scholar 

  77. Troiano AR, Elbaz A, Lohmann E, Belarbi S, Vidailhet M, Bonnet AM, et al. Low disease risk in relatives of north african lrrk2 Parkinson disease patients. Neurology. 2010;75(12):1118–9.

    Article  CAS  PubMed  Google Scholar 

  78. Change N, Mercier G, Lucotte G. Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects. Genet Test. 2008;12(3):333–9.

    Article  CAS  PubMed  Google Scholar 

  79. Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Durr A, et al. LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. Am J Hum Genet. 2005;77(2):330–2.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  80. Zabetian CP, Hutter CM, Yearout D, Lopez AN, Factor SA, Griffith A, et al. LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. Am J Hum Genet. 2006;79(4):752–8.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  81. Warren L, Gibson R, Ishihara L, Elango R, Xue Z, Akkari A, et al. A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson’s disease. Parkinsonism Relat Disord. 2008;14(1):77–80.

    Article  CAS  PubMed  Google Scholar 

  82. Healy DG, Wood NW, Schapira AH. Test for LRRK2 mutations in patients with Parkinson’s disease. Pract Neurol. 2008;8(6):381–5.

    Article  CAS  PubMed  Google Scholar 

  83. Lucotte G, David D, Change N. New contribution on LRRK2 G2019S mutation associated to Parkinson’s disease: age estimation of common founder event of old age in Moroccan Berbers. Int J Mod Anthropol. 2012;5:11–22.

    Google Scholar 

  84. Dieterlen F, Lucotte G. Origin of the G2019S mutation associated to Parkinson’s disease in Europeans and in North Africans. Int J Mod Anthropol. 2010;3:81–96.

    Google Scholar 

  85. Chaabani H, Cox DW. Genetic characterization and origin of Tunisian Berbers. Hum Hered. 1988;38(5):308–16.

    Article  CAS  PubMed  Google Scholar 

  86. Chaabani H, Sanchez-Mazas A, Sallami SF. Genetic differentiation of Yemeni people according to rhesus and Gm polymorphisms. Ann Genet. 2000;43(3–4):155–62.

    Article  CAS  PubMed  Google Scholar 

  87. Abdennaji GB, Loueslati BY, Buhler S, Hmida S, Ennafaa H, Khodjet-Elkhil H, et al. HLA class II genetic diversity in southern Tunisia and the Mediterranean area. Int J Immunogenet. 2006;33(2):93–103.

    Article  Google Scholar 

  88. Ennafaa H, Amor MB, Yacoubi-Loueslati B, Khodjet el-khil H, Gonzalez-Perez E, Moral P, et al. Alu polymorphisms in Jerba Island population (Tunisia): comparative study in Arab and Berber groups. Ann Hum Biol. 2006;33(5–6):634–40.

    Article  PubMed  Google Scholar 

  89. Farrer MJ, Gibson R, Hentati F. The ancestry of LRRK2 Gly2019Ser parkinsonism (Authors’ reply). Lancet Neurol. 2009;7:770.

    Article  Google Scholar 

  90. Al-Din NAS, Wriekat A, Mubaidin A, Dasouki M, Hiari M. Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome. Acta Neurol Scand. 1994;89(5):347–52.

    Article  Google Scholar 

  91. Williams DR, Hadeed A, Al-Din AS, Wreikat AL, Lees AJ. Kufor Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia. Mov Disord. 2005;20(10):1264–71.

    Article  PubMed  Google Scholar 

  92. Hampshire DJ, Roberts E, Crow Y, Bond J, Mubaidin A, Wriekat AL, et al. Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36. J Med Genet. 2001;38(10):680–2.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  93. Ramirez A, Heimbach A, Grundemann J, Stiller B, Hampshire D, Cid LP, et al. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nat Genet. 2006;38(10):1184–91.

    Article  CAS  PubMed  Google Scholar 

  94. Benamer HT, de Silva R. LRRK2 G2019S in the North African population: a review. Eur Neurol. 2010;63(6):321–5.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgment

Some of the text in this chapter which is related to LRRK 2 (PARK 8) have been taken, after adjustments, from a paper published previously by the author [94]. Permission for reproduction was obtained from Karger publishers.

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 2014 Springer International Publishing Switzerland

About this chapter

Cite this chapter

Benamer, H.T.S. (2014). Parkinson’s Disease. In: Neurological Disorders in the Arab World. Springer, Cham. https://doi.org/10.1007/978-3-319-07257-9_6

Download citation

  • DOI: https://doi.org/10.1007/978-3-319-07257-9_6

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-07256-2

  • Online ISBN: 978-3-319-07257-9

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics