Literature DB >> 26413584

Epilepsy genetics in Africa: challenges and future perspectives.

Guida Landouré1, Youssoufa Maiga2, Oumar Samassékou3, Karamoko Nimaga4, Mahamadou Traoré5, Kenneth H Fischbeck6.   

Abstract

Despite the diversity of the African population, genetic studies, of epilepsy in particular, have been limited, especially in sub-Saharan Africa. In recent years, with the regression of infectious diseases in developing countries, the focus has shifted more towards non communicable disorders. The prevalence of epilepsy in Africa is higher compared to other continents. Although this has been attributed to the high rate of infectious diseases, genetic contributions should not be ignored. Research in genetic epilepsy in Africa could well benefit from the decreasing cost of genetic analysis, and could contribute to further our knowledge on the spectrum of these diseases in Africa. The growing collaboration between African research institutions and those of developed countries offers a unique opportunity to boost research in Africa and improve our global understanding of human disease, thus leading to the development of better therapeutic approaches.

Entities:  

Keywords:  Africa; Epilepsy; Genetics

Year:  2014        PMID: 26413584      PMCID: PMC4580280     

Source DB:  PubMed          Journal:  North Afr Middle East Epilepsy J


  19 in total

1.  First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene.

Authors:  S Baulac; G Huberfeld; I Gourfinkel-An; G Mitropoulou; A Beranger; J F Prud'homme; M Baulac; A Brice; R Bruzzone; E LeGuern
Journal:  Nat Genet       Date:  2001-05       Impact factor: 38.330

2.  New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures.

Authors:  N Fendri-Kriaa; F Kammoun; I Hadj Salem; C Kifagi; E Mkaouar-Rebai; I Hsairi; A Rebai; C Triki; F Fakhfakh
Journal:  Eur J Neurol       Date:  2010-10-06       Impact factor: 6.089

3.  A novel exon 3 mutation in a Tunisian patient with Lafora's disease.

Authors:  H Mrabet Khiari; G Lesca; A Malafosse; A Mrabet
Journal:  J Neurol Sci       Date:  2011-03-03       Impact factor: 3.181

4.  Clinical and genetic aspects of seizure disorders prevalent in an isolated African population.

Authors:  L Jilek-Aall; W Jilek; J R Miller
Journal:  Epilepsia       Date:  1979-12       Impact factor: 5.864

5.  A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

Authors:  O K Steinlein; J C Mulley; P Propping; R H Wallace; H A Phillips; G R Sutherland; I E Scheffer; S F Berkovic
Journal:  Nat Genet       Date:  1995-10       Impact factor: 38.330

Review 6.  Genes and mutations in human idiopathic epilepsy.

Authors:  Ortrud K Steinlein
Journal:  Brain Dev       Date:  2004-06       Impact factor: 1.961

7.  [Unverricht-Lündborg disease: clinical and electrophysiologic study of 19 Maghreb families].

Authors:  R Gouider; S Ibrahim; M Fredj; A Gargouri; H Saïdi; R Ouezzani; A Malafosse; M Yahiaoui; D Grid; A Mrabet
Journal:  Rev Neurol (Paris)       Date:  1998-07       Impact factor: 2.607

8.  Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

Authors:  R H Wallace; D W Wang; R Singh; I E Scheffer; A L George; H A Phillips; K Saar; A Reis; E W Johnson; G R Sutherland; S F Berkovic; J C Mulley
Journal:  Nat Genet       Date:  1998-08       Impact factor: 38.330

9.  Results of an action-research on epilepsy in rural Mali.

Authors:  Elisa Bruno; Karamoko Nimaga; Ibrahima Foba; Philippe Vignoles; Pierre Genton; Ogobara Doumbo; Daniel Gérard; Pierre-Marie Preux; Guy Farnarier
Journal:  PLoS One       Date:  2012-08-31       Impact factor: 3.240

10.  Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease.

Authors:  M Traoré; G Landouré; W Motley; M Sangaré; K Meilleur; S Coulibaly; S Traoré; B Niaré; F Mochel; A La Pean; A Vortmeyer; H Mani; K H Fischbeck
Journal:  Neurogenetics       Date:  2009-03-26       Impact factor: 2.660

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  3 in total

1.  The elusive ideal of inclusiveness: lessons from a worldwide survey of neurologists on the ethical issues raised by whole-genome sequencing.

Authors:  Thierry Hurlimann; Iris Jaitovich Groisman; Béatrice Godard
Journal:  BMC Med Ethics       Date:  2017-04-11       Impact factor: 2.652

2.  Genetics and genomic medicine in Mali: challenges and future perspectives.

Authors:  Guida Landouré; Oumar Samassékou; Mahamadou Traoré; Katherine G Meilleur; Cheick Oumar Guinto; Barrington G Burnett; Charlotte J Sumner; Kenneth H Fischbeck
Journal:  Mol Genet Genomic Med       Date:  2016-03-17       Impact factor: 2.183

3.  Clinical Application of Epilepsy Genetics in Africa: Is Now the Time?

Authors:  Alina I Esterhuizen; Gemma L Carvill; Rajkumar S Ramesar; Symon M Kariuki; Charles R Newton; Annapurna Poduri; Jo M Wilmshurst
Journal:  Front Neurol       Date:  2018-05-02       Impact factor: 4.003

  3 in total

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