Background: Africans are underrepresented in Huntington's disease (HD) research. A European ancestor was postulated to have introduced the mutant Huntingtin (mHtt) gene to the continent; however, recent work has shown the existence of a unique Htt haplotype in South-Africa specific to indigenous Africans.
Objective: We aimed to investigate the CAG trinucleotide repeats expansion in the Htt gene in a geographically diverse cohort of patients with chorea and unaffected controls from sub-Saharan Africa.
The burden of encephalitis and its associated viral etiology is poorly described in Africa. Moreover, neurological manifestations of COVID-19 are increasingly reported in many countries, but less so in Africa. Our prospective study aimed to characterize the main viral etiologies of patients hospitalized for encephalitis in two hospitals in Dakar.
View Article and Find Full Text PDFBackground: Movement disorders have different prevalence in different regions and they are little studied in Africa.
Objectives: Evaluate the prevalence and determine the spectrum of movement disorders in the first specialized center in Senegal.
Methods: It was a prospective study over on 18 months in adult outpatient clinic.
Background: Neuromyelitis optica (NMO) is an autoimmune disease of the central nervous system. In Sub-Saharan Africa, publications are rare and deal with isolated cases. Our goal was to analyze the characteristics of NMO spectrum disorders in a Senegalese cohort compiled in Dakar.
View Article and Find Full Text PDFBackground: Epilepsy remains a major public health problem especially in developing countries where access to new therapies remains limited.
Objective: The aim of this work was to study the socio-demographic profile of patients living with epilepsy in Dakar and supported.
Methods: We conducted a cross-sectional study over a period of eight months from November 2009 to June 2010 at Fann University Hospital and Health Center Pikine through research on adherence.