Precious time saved for both the practitioner and the patient!
Detect as soon as possible a patient suffering from a rare disease and accelerate his referral to an expert center to confirm the diagnosis.
A digital solution born from the open innovation process started in 2018 with the active contribution of 37 actors of the French health ecosystem.
|DISEASE||Diagnosis lag time
for 50% of patients
|Diagnosis lag time
for 75% of patients
|Cystic fibrosis||1.5 months||15 months|
|Tuberous sclerosis||4 months||3 years|
|Duchenne muscular dystrophy||12 months||3 years|
|Prader willi syndrome||18 months||6.1 years|
|Marfan syndrome||18 months||11.1 years|
|Fragile X Syndrome||2.8 years||5.3 years|
|Ehlers-Danlos syndrome||14 years||28 years|
Source White paper UNIR – Innovating together to reduce diagnostic delay in rare diseases, 2018
Health actors gather to find innovative solutions to reduce diagnostic delay in rare diseases.