Literature DB >> 34824573

[Clinical and laboratory features of recessive Limb Girdle Muscular dystrophies in the Department Neurology of University Hospital of Point G].

Th Coulibaly1,2, A J Ouabo1, G Landouré1,2, H O Bah2,3, L Cissé1, S H Diallo2,4, S Diallo4, O Samassékou2, A B Maïga1, F Kané2, A Yalcouyé2, A Taméga2, A Bocoum2, M E Dembélé2, A Témé1, C O Sidibé1, A K Cissé2, O Traoré2, M Traoré5, C O Guinto1,2.   

Abstract

INTRODUCTION: Limb-Girdle Muscular dystrophies (LGMD) is a group of inherited diseases characterized by predominantly proximal and limb muscle weakness. These are rare diseases that have not been well studied in sub-saharan Africa. The aim of our was the clinical and paraclinical characterization of patients with recessive LGMD at the Department of Neurology of the Teaching Hospital of Point G. PATIENTS AND METHODS: We conducted a longitudinal prospective study which took place from March 2014 to May 2019. Patients with recessive LGMD phenotype were enrolled. Sociodemographic, clinical and laboratory data were analyzed.
RESULTS: We enrolled 46 families (67 patients), i.e. a frequency of 16.7% among the neurodegenerative diseases seen in the service. Among them, 45.6% came from the Sikasso region. Autosomal recessive inheritance pattern was suspected in 67.4% of the families. Symptoms appeared mainly in the first decade of life. Proximal muscle weakness was found in almost all patients. Cardiac examination showed dilated cardiomyopathy in 4.5% of cases.
CONCLUSION: Limb-Girdle muscular dystrophy is a disabling disease that is found in Mali. Further study of these cases could elucidate the underlying genetic defects.

Entities:  

Keywords:  LGMD; Mali; Teaching Hospital of Point G; clinic

Year:  2021        PMID: 34824573      PMCID: PMC8612446     

Source DB:  PubMed          Journal:  Health Sci Dis        ISSN: 1684-2782


  11 in total

1.  Novel mutation in the ATM gene in a Malian family with ataxia telangiectasia.

Authors:  Guida Landouré; Fanny Mochel; Katherine Meilleur; Madani Ly; Modibo Sangaré; Nouhoum Bocoum; Koumba Bagayoko; Thomas Coulibaly; Amadou M Sarr; Hamidou O Bâ; Souleymane Coulibaly; Cheick O Guinto; Mahamadou Touré; Moussa Traoré; Kenneth H Fischbeck
Journal:  J Neurol       Date:  2012-11-11       Impact factor: 4.849

2.  Systemic AAV-Mediated β-Sarcoglycan Delivery Targeting Cardiac and Skeletal Muscle Ameliorates Histological and Functional Deficits in LGMD2E Mice.

Authors:  Eric R Pozsgai; Danielle A Griffin; Kristin N Heller; Jerry R Mendell; Louise R Rodino-Klapac
Journal:  Mol Ther       Date:  2017-03-09       Impact factor: 11.454

3.  Diagnosis and treatment of limb-girdle and distal dystrophies: Payment policy perspectives.

Authors:  Raghav Govindarajan; Katie M Shepard; Lyell K Jones
Journal:  Neurol Clin Pract       Date:  2015-10

4.  Cognitive and psychological profile of a Tunisian population of limb girdle muscular dystrophy.

Authors:  N Miladi; J P Bourguignon; F Hentati
Journal:  Neuromuscul Disord       Date:  1999-07       Impact factor: 4.296

5.  TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophy.

Authors:  Roula Ghaoui; Tatiana Benavides; Monkol Lek; Leigh B Waddell; Simranpreet Kaur; Kathryn N North; Daniel G MacArthur; Nigel F Clarke; Sandra T Cooper
Journal:  Neuromuscul Disord       Date:  2016-05-24       Impact factor: 4.296

6.  A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory loss.

Authors:  Cheick O Guinto; Salimata Diarra; Salimata Diallo; Lassana Cissé; Thomas Coulibaly; Seybou H Diallo; Abdoulaye Taméga; Ke-Lian Chen; Alice B Schindler; Koumba Bagayoko; Assiatou Simaga; Craig Blackstone; Kenneth H Fischbeck; Guida Landouré
Journal:  Ann Clin Transl Neurol       Date:  2017-03-21       Impact factor: 4.511

7.  A novel mutation in the GARS gene in a Malian family with Charcot-Marie-Tooth disease.

Authors:  Abdoulaye Yalcouyé; Seybou H Diallo; Thomas Coulibaly; Lassana Cissé; Salimata Diallo; Oumar Samassékou; Salimata Diarra; Dramane Coulibaly; Mohamed Keita; Cheick O Guinto; Kenneth Fischbeck; Guida Landouré
Journal:  Mol Genet Genomic Med       Date:  2019-06-07       Impact factor: 2.183

8.  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
Journal:  Ann Neurol       Date:  2014-04-02       Impact factor: 10.422

9.  A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies.

Authors:  Dorota Monies; Hindi N Alhindi; Mohamed A Almuhaizea; Mohamed Abouelhoda; Anas M Alazami; Ewa Goljan; Banan Alyounes; Dyala Jaroudi; Abdulelah AlIssa; Khalid Alabdulrahman; Shazia Subhani; Mohamed El-Kalioby; Tariq Faquih; Salma M Wakil; Nada A Altassan; Brian F Meyer; Saeed Bohlega
Journal:  Hum Genomics       Date:  2016-09-27       Impact factor: 4.639

10.  The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients.

Authors:  Liang Wang; Victor Wei Zhang; Shaoyuan Li; Huan Li; Yiming Sun; Jing Li; Yuling Zhu; Ruojie He; Jinfu Lin; Cheng Zhang
Journal:  Orphanet J Rare Dis       Date:  2018-08-14       Impact factor: 4.123

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