Literature DB >> 22109722

Genetic testing and counseling for hereditary neurological diseases in Mali.

Katherine Gloria Meilleur1, Souleymane Coulibaly, Moussa Traoré, Guida Landouré, Alison La Pean, Modibo Sangaré, Fanny Mochel, Siona Traoré, Kenneth H Fischbeck, Hae-Ra Han.   

Abstract

As genetic advances become incorporated into health care delivery, disparities between developing and developed countries may become greater. By addressing genetic health care needs and specific differences of developing countries, these disparities may be mitigated. We sought to describe the attitudes and knowledge of subjects with hereditary neurological diseases in Mali before and after receiving genetic testing and counseling for the first time. A questionnaire of attitudes and knowledge items was adapted and piloted for use in Mali. We found that the majority of subjects had positive attitudes toward genetic testing and counseling, both before and afterwards. Subjects responded to approximately half of the knowledge questions regarding hereditary transmission correctly before and after genetic testing and counseling. Neither overall attitudes nor knowledge scores changed significantly from baseline. Concerns about confidentiality were expressed by the majority of subjects. These findings indicate that, despite limited knowledge of patterns of inheritance, Malians understood the sensitive nature of this information and were favorable toward receiving genetic testing and counseling for diagnostic and prognostic purposes.

Entities:  

Year:  2011        PMID: 22109722      PMCID: PMC3186021          DOI: 10.1007/s12687-011-0038-0

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  32 in total

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Journal:  Ophthalmic Genet       Date:  2007-09       Impact factor: 1.803

8.  Attitude toward genetic testing for cancer risk in Istanbul.

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Journal:  Haemophilia       Date:  2007-09       Impact factor: 4.287

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Journal:  Health Sci Dis       Date:  2021-11

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4.  Neuropsychiatric and socio-cultural aspects in a Malian family with spinocerebellar ataxia.

Authors:  Souleymane P Coulibaly; Souleymane Coulibaly; Hammadoun A Sango; Lassana Cissé; Fatoumata I Maïga; Boubacar Maïga; Salimata Diarra; Seybou H Diallo; Thomas Coulibaly; Mahamadou Traoré; Cheick O Guinto; Baba Koumaré; Guida Landouré
Journal:  Ann Med Psychol (Paris)       Date:  2019-03-18       Impact factor: 0.380

Review 5.  Retinoblastoma genetics in India: From research to implementation.

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Journal:  Indian J Ophthalmol       Date:  2015-03       Impact factor: 1.848

6.  Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians?

Authors:  Modibo Sangare; Ilo Dicko; Cheick Oumar Guinto; Adama Sissoko; Kekouta Dembele; Youlouza Coulibaly; Siaka Y Coulibaly; Guida Landoure; Abdallah Diallo; Mamadou Dolo; Housseini Dolo; Boubacar Maiga; Moussa Traore; Mamadou Karembe; Kadiatou Traore; Amadou Toure; Mariam Sylla; Arouna Togora; Souleymane Coulibaly; Sékou Fantamady Traore; Brant Hendrickson; Katherine Bricceno; Alice B Schindler; Angela Kokkinis; Katherine G Meilleur; Hammadoun Ali Sangho; Brehima Diakite; Yaya Kassogue; Yaya Ibrahim Coulibaly; Barrington Burnett; Youssoufa Maiga; Seydou Doumbia; Kenneth H Fischbeck
Journal:  eNeurologicalSci       Date:  2016-01-04

7.  Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa.

Authors:  Modibo Sangaré; Brant Hendrickson; Hammadoun Ali Sango; Kelian Chen; Jonathan Nofziger; Abdelbasset Amara; Amalia Dutra; Alice B Schindler; Aldiouma Guindo; Mahamadou Traoré; George Harmison; Evgenia Pak; Fatoumata N'Go Yaro; Katherine Bricceno; Christopher Grunseich; Guibin Chen; Manfred Boehm; Kristen Zukosky; Nouhoum Bocoum; Katherine G Meilleur; Fatoumata Daou; Koumba Bagayogo; Yaya Ibrahim Coulibaly; Mahamadou Diakité; Michael P Fay; Hee-Suk Lee; Ali Saad; Moez Gribaa; Andrew B Singleton; Youssoufa Maiga; Sungyoung Auh; Guida Landouré; Rick M Fairhurst; Barrington G Burnett; Thomas Scholl; Kenneth H Fischbeck
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8.  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

Review 9.  Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies.

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10.  DMD-related muscular dystrophy in Cameroon: Clinical and genetic profiles.

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