Rare Diseases
Get a global overview and learn all about changing world of Rare diseases
Science in Rare Diseases
Get a 360º view and stay updated on Rare diseases with content selected for you
.webp/jcr:content/gaucher-thumb%20(2).webp)
How To Diagnose LSDs?
Learn more about early diagnosis of lysosomal storage disorders: Fabry disease, Pompe Disease, Gaucher disease, Acid Sphingomyelinase Deficiency (ASMD, also known as Niemann-Pick Type A/B), mucopolysaccharidoses (MPSs).
Inspiration and innovation
Get inspired and stay at the forefront of innovation with the following resources
How To Diagnose LSDs?
Learn more about early diagnosis of lysosomal storage disorders: Fabry disease, Pompe Disease, Gaucher disease, Acid Sphingomyelinase Deficiency (ASMD, also known as Niemann-Pick Type A/B), mucopolysaccharidoses (MPSs).
An overview of Lysosomal Storage Disorders & Sanofi`s Commitment to the Development and Provision of Treatments
Experts recommendations on Late Onset Pompe Disease (LOPD) differential diagnosis from GCC
Expert Group Consensus From The Arabian Peninsula On The Diagnosis Of Late Onset Pompe Disease (LOPD)
Expert Group Consensus From The Arabian Peninsula On The Diagnosis Of Late Onset Pompe Disease for orthopedists
Events
Stay up to date and register for the latest events and view webinar recordings.
.png/jcr:content/thumb-events-rd%20(1).png)
