Literature DB >> 22831947

Inherited polyglutamine spinocerebellar ataxias in South Africa.

D C Smith1, A Bryer, L M Watson, L J Greenberg.   

Abstract

OBJECTIVE: To determine the frequency and distribution of polyglutamine spinocerebellar ataxias (SCAs) from referrals over a 24-year period to the National Health Laboratory Service (NHLS) in South Africa (SA).
METHODS: Paper-based clinical reports in the University of Cape Town laboratory and the NHLS electronic patient record database spanning a 24-year period were mined for information regarding the molecular diagnosis, ethnicity and CAG repeat length for individuals referred for molecular genetic testing for the polyglutamine SCAs.
RESULTS: SCA1 and 7 are the most frequent types of polyglutamine SCA in the SA patient population, followed by SCA2, 3 and 6. SCA1 is the most common type in the coloured, white and Indian populations, whereas the majority of indigenous black African patients are affected with SCA7 and 2. Of individuals tested, 22% were found to be positive for one of the polyglutamine SCAs.
CONCLUSION: Although trends in the frequency and distribution of the polyglutamine SCAs in SA have not changed significantly since our previous study in 2003, they differ remarkably from those reported elsewhere, and reflect the unique genetic and demographic background of SA. The provision of accurate and complete patient information and family history is crucial to the diagnostic process, to enable comprehensive epidemiological studies and assist in developing therapeutic and patient management strategies.

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Year:  2012        PMID: 22831947     DOI: 10.7196/samj.5521

Source DB:  PubMed          Journal:  S Afr Med J


  9 in total

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2.  Allele-specific silencing of mutant Ataxin-7 in SCA7 patient-derived fibroblasts.

Authors:  Janine Scholefield; Lauren Watson; Danielle Smith; Jacquie Greenberg; Matthew J A Wood
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Journal:  Cerebellum       Date:  2014-02       Impact factor: 3.847

Review 4.  Neurogenomics in Africa: Perspectives, progress, possibilities and priorities.

Authors:  Rufus O Akinyemi; Mayowa O Owolabi; Tolulope Oyeniyi; Bruce Ovbiagele; Donna K Arnett; Hemant K Tiwari; Richard Walker; Adesola Ogunniyi; Raj N Kalaria
Journal:  J Neurol Sci       Date:  2016-05-06       Impact factor: 3.181

5.  Molecular and electrophysiological features of spinocerebellar ataxia type seven in induced pluripotent stem cells.

Authors:  Richard J Burman; Lauren M Watson; Danielle C Smith; Joseph V Raimondo; Robea Ballo; Janine Scholefield; Sally A Cowley; Matthew J A Wood; Susan H Kidson; Leslie J Greenberg
Journal:  PLoS One       Date:  2021-02-24       Impact factor: 3.240

6.  Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7.

Authors:  Xuan Zou; Fengxia Yao; Fengrong Li; Shijing Wu; Hui Li; Zixi Sun; Tian Zhu; Xing Wei; Donghui Li; Ruifang Sui
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Journal:  IBRO Neurosci Rep       Date:  2021-02-10

8.  Spinocerebellar ataxia type-7: Report of a family in Northwest Nigeria.

Authors:  Nura Hamidu Alkali; Sunday A Bwala; Saeed A Alimi; Shyngle I Oyakhire
Journal:  Ann Afr Med       Date:  2016 Apr-Jun

9.  Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.

Authors:  Masharip Atadzhanov; Danielle C Smith; Mwila H Mwaba; Omar K Siddiqi; Alan Bryer; L Jacquie Greenberg
Journal:  Cerebellum Ataxias       Date:  2017-11-29
  9 in total

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