Literature DB >> 21509270

Huntington disease (chorea) in the middle East.

Euan M Scrimgeour1.   

Abstract

Huntington disease (HD) has been reported in Arab families in several Middle East countries including Saudi Arabia, Oman, Syria, Lebanon, and Egypt and in non-Arab populations in other countries in the region. It is probably under-reported, and until now, has not been recorded in Yemen, the United Arab Emirates, Jordan or in Iraq. The Middle East has always been on the crossroads of trade and travel, and HD was probably introduced to some of these countries in previous times. The prevalence rate in Middle Eastern Arabs is estimated to vary from 3 to 4 per 100,000. Although the HD gene which codes for the protein huntingtin has been identified, the function of this protein is not known. At present, no treatment has been found to delay the onset of HD or to treat it effectively. Although relatively rare, HD has increasingly become a focus of international gene research, with the support and collaboration of the International Huntington Association (IHA). The IHA has been represented in Saudi Arabia and Oman.

Entities:  

Keywords:  Arab race; Chorea; Huntington; Middle East

Year:  2009        PMID: 21509270      PMCID: PMC3074759     

Source DB:  PubMed          Journal:  Sultan Qaboos Univ Med J        ISSN: 2075-051X


  25 in total

Review 1.  Transgenic models of Huntington's disease.

Authors:  K Sathasivam; C Hobbs; L Mangiarini; A Mahal; M Turmaine; P Doherty; S W Davies; G P Bates
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-06-29       Impact factor: 6.237

Review 2.  Huntingtin and its role in neuronal degeneration.

Authors:  Shi-Hua Li; Xiao-Jiang Li
Journal:  Neuroscientist       Date:  2004-10       Impact factor: 7.519

3.  The long-term effect of tetrabenazine in the management of Huntington disease.

Authors:  Alfonso Fasano; Federica Cadeddu; Arianna Guidubaldi; Carla Piano; Francesco Soleti; Paola Zinzi; Anna Rita Bentivoglio
Journal:  Clin Neuropharmacol       Date:  2008 Nov-Dec       Impact factor: 1.592

Review 4.  Pathophysiology of Huntington's disease: from huntingtin functions to potential treatments.

Authors:  Emmanuel Roze; Frédéric Saudou; Jocelyne Caboche
Journal:  Curr Opin Neurol       Date:  2008-08       Impact factor: 5.710

5.  Distribution of CAG repeats in normal and Huntington's disease patients in Israel.

Authors:  E Gazit; L Lubomirov; O Munakov; A Topper; M Frydman; K Fried; Z Borochovitz; N Dangoor; A Bogolubov; H J Carp
Journal:  Clin Genet       Date:  1998-09       Impact factor: 4.438

6.  Juvenile onset Huntington's disease in an Omani child with asymptomatic, at risk parents.

Authors:  E M Scrimgeour; R L Koul; P R Chand; J K Tharakan; C A Frew
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

7.  A polymorphic DNA marker genetically linked to Huntington's disease.

Authors:  J F Gusella; N S Wexler; P M Conneally; S L Naylor; M A Anderson; R E Tanzi; P C Watkins; K Ottina; M R Wallace; A Y Sakaguchi
Journal:  Nature       Date:  1983 Nov 17-23       Impact factor: 49.962

Review 8.  Pharmacological management of Huntington's disease: an evidence-based review.

Authors:  Raphael M Bonelli; Gregor K Wenning
Journal:  Curr Pharm Des       Date:  2006       Impact factor: 3.116

9.  Huntington disease in black Zimbabwean families living near the Mozambique border.

Authors:  E M Scrimgeour; J W Pfumojena
Journal:  Am J Med Genet       Date:  1992-12-01

10.  Randomized controlled trial of ethyl-eicosapentaenoic acid in Huntington disease: the TREND-HD study.

Authors: 
Journal:  Arch Neurol       Date:  2008-12
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  2 in total

1.  Clinical and genetic data of Huntington disease in Moroccan patients.

Authors:  Ahmed Bouhouche; Wafaa Regragui; Hind Lamghari; Khadija Khaldi; Nazha Birouk; Safaa Lytim; Soufiane Bellamine; Yamna Kriouile; Naima Bouslam; El Hachmia Ait Ben Haddou; Mustapha Alaoui Faris; Ali Benomar; Mohamed Yahyaoui
Journal:  Afr Health Sci       Date:  2015-12       Impact factor: 0.927

2.  Huntington's disease among immigrant groups and Swedish-born individuals: a cohort study of all adults 18 years of age and older in Sweden.

Authors:  Per Wändell; Sten Fredrikson; Axel C Carlsson; Xinjun Li; Jan Sundquist; Kristina Sundquist
Journal:  Neurol Sci       Date:  2021-01-30       Impact factor: 3.307

  2 in total

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