General
RW2022SIN353A103
01/09/2022 - 31/08/2024
Epilepsy is one of the most common chronic neurological disorders affecting 70 million people worldwide of whom 85% live in low- and middle-income countries. The epilepsy treatment gap, which includes the diagnosis gap, amounts to 80% in sub-Saharan Africa (SSA). The prevalence in Rwanda is amongst the highest of SSA, estimated at 4.9%, with an epilepsy treatment gap of 91.5% due to diagnostic and therapeutic limitations in rural areas. However, causes underlying the high prevalence in Rwanda have never thoroughly been identified. In Africa, epilepsy is often secondary to perinatal insults, early-life trauma or central nervous system infections. Nonetheless, the cause of epilepsy in over 60% of African children is unknown, suggesting a possible genetic origin. Early-onset epilepsies (EOE) are an important cause for childhood morbidity in the African continent since in 80% of people living with epilepsy in SSA, the first seizure appears before 18 years of age. Thus, the relevance of knowledge on epilepsy genetics in EOE to patient care is evident, especially as early genetic testing can confirm the diagnosis and direct treatment, potentially improving prognosis and quality of life. However, access to human genomic testing is non-existent in Rwanda. Therefore, this project will 1) strengthen the research capacity on EOE by establishing an interdisciplinary research group supporting neurologists, geneticists, residents and PhD students in driving research on the genetic causes of EOE in Rwanda, and 2) improve capacity for accurate diagnosis, treatment and comprehensive care in people with EOE by a) the implementation of genetic testing, b) the educative training of community and primary healthcare providers, and c) the improvement of access to community-based rehabilitation in remote areas. The goal is to create capacity for accessible genetic services for epilepsy in Rwanda, and beyond, that will improve diagnostics, treatment and quality of comprehensive care provided to patients living with epilepsy by using a community-based approach.
General information
Title
SI-Improving diagnostics, treatment and comprehensive care in people living with early-onset epilepsy in Rwanda
ID
XM-DAC-2-10-10609
Start date
End date
Activity status
Implementation
Budget
€40.839
Actor
VLIR-UOS - Vlaamse Interuniversitaire Raad - Flemish Interuniversity Council
Country
RWANDA
Sector
Health - Non-communicable diseases (NCD) - Research for prevention and control of NCDs
Aid type
Core support to NGOs, other private bodies, PPPs and research institutes
Priority partner country
Yes
Fragile state
Yes
Least developed country
Yes
Budgetline
54 41 452501 Steun aan VLIR mbt de realisatie van de doelen van de gemeenschappelijke strategische kaders
Finance type
GRANT
Tied status
No
Flow type
ODA
Documents
Documents