Literature DB >> 32431322

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

Souleymane P Coulibaly1,2, Souleymane Coulibaly1,2, Hammadoun A Sango1, Lassana Cissé3, Fatoumata I Maïga1, Boubacar Maïga3, Salimata Diarra3, Seybou H Diallo1,4, Thomas Coulibaly1,2, Mahamadou Traoré1,5, Cheick O Guinto1,2, Baba Koumaré1,2, Guida Landouré1,2.   

Abstract

INTRODUCTION: Spino-cerebellar ataxia or SCA are dominant neurological diseases caused by mutations in several genes. According to social and cultural contexts, especially in populations with low education level, the advent of such diseases might generate other kinds of suffering beside those caused by the physical impairment and disability. The aim of this work was to determine the impact of this disease in patients and their relatives.
METHODS: It was a qualitative approach carried out through semi-directive clinical interviews, neuropsychiatric observations and the administration of the Hamilton depression scale.
RESULTS: The study included a polygamous family in which mothers had 10 and 12 maternities. Neurological manifestations concerned four children of the same siblings and the father in a subtle form. The mother of these children was designated as responsible for the transmission of the disease and presented a reaction depression. Irritability, anxiety and depression reactions were observed in two patients and an unaffected brother. The advent of the disease was associated to the hatching of a latent familial conflict related to the father's status that has been established only after four years.
CONCLUSION: In a social and cultural setting of polygamy, the advent of dominant ataxia with anticipation might revive latent familial conflicts and have psychological and social repercussions on the affected individuals and their relatives.

Entities:  

Keywords:  Clinical cas; Depression; Family; Heridity; Neurological disease; Social context; Spino-cerebellar ataxia

Year:  2019        PMID: 32431322      PMCID: PMC7236554          DOI: 10.1016/j.amp.2018.02.018

Source DB:  PubMed          Journal:  Ann Med Psychol (Paris)        ISSN: 0003-4487            Impact factor:   0.380


  6 in total

1.  Genetic testing and counseling for hereditary neurological diseases in Mali.

Authors:  Katherine Gloria Meilleur; Souleymane Coulibaly; Moussa Traoré; Guida Landouré; Alison La Pean; Modibo Sangaré; Fanny Mochel; Siona Traoré; Kenneth H Fischbeck; Hae-Ra Han
Journal:  J Community Genet       Date:  2011-02-22

Review 2.  Infantile spinocerebellar ataxia type 7: Case report and a review of the literature.

Authors:  Karina Carvalho Donis; Eduardo Preusser Mattos; André Anjos Silva; Gabriel Vasata Furtado; Maria Luiza Saraiva-Pereira; Laura Bannach Jardim; Jonas Alex Saute
Journal:  J Neurol Sci       Date:  2015-05-05       Impact factor: 3.181

3.  Clinical and genetic analysis of spinocerebellar ataxia in Mali.

Authors:  M Traoré; T Coulibaly; K G Meilleur; A La Pean; M Sangaré; G Landouré; F Mochel; M Karambé; C O Guinto; K H Fischbeck
Journal:  Eur J Neurol       Date:  2011-03-21       Impact factor: 6.089

Review 4.  Cerebellar ataxias.

Authors:  Mario Manto; Daniele Marmolino
Journal:  Curr Opin Neurol       Date:  2009-08       Impact factor: 5.710

5.  [Psychosocial impact of sickle cell disease in the parents of children living in Kinshasa, Democratic Republic of Congo: a qualitative study].

Authors:  Evariste Luboya; Jean-Christophe Bukasa Tshilonda; Mathilde Bothale Ekila; Michel Ntetani Aloni
Journal:  Pan Afr Med J       Date:  2014-09-02

Review 6.  Hereditary ataxias: overview.

Authors:  Suman Jayadev; Thomas D Bird
Journal:  Genet Med       Date:  2013-03-28       Impact factor: 8.822

  6 in total

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