Early Diagnosis & Referral Pathways
Strengthening clinical recognition and referral systems for rare and genetic conditions.
Delayed diagnosis is one of the greatest burdens faced by people living with rare diseases. In Africa, this delay is often compounded by limited awareness, overlapping symptoms with common conditions, and the absence of structured referral pathways.
ARRC focuses on improving early recognition of rare and genetic diseases by promoting informed clinical reasoning, appropriate use of diagnostic tools, and timely referral to specialized services. Our work emphasizes practical, context-appropriate approaches that can be implemented within existing health systems.
By supporting earlier diagnosis, we aim to reduce mismanagement, prevent avoidable complications, and shorten the diagnostic journey for patients and families.
Early diagnosis is not a luxury, it is a medical and ethical necessity.