Take Care of Rare
Timely diagnosis of patients with a rare genetic disease is a real challenge.
Through this podcast series, you will learn more about how we inform/support healthcare professionals to accelerate early detection.
This content is intended for healthcare professionals in Belgium and Luxembourg and is brought to you by Takeda Belgium.
This podcast series on Fabry Disease with 7 episodes has been co-created with your colleagues with focus on 4 areas:
1. Rare Diseases with Prof. Dr. David Cassiman:
a. episodes 1 : the importance of early diagnosis
b. episode 2: the referral trajectory
2. Cardiology with Prof. Dr. T. Robyns:
a. episode 3: Fabry Disease and the Heart
3. Nephrology with Dr. W. Terryn & Dr. G. De Schoenmakere:
a. episodes 4: Fabry Disease and the kidney #1
b. episode 5: Fabry Disease and the kidney #2
4. Neurology with Dr. D. Hemelsoet & Dr. J. Demeestere:
a. episode 6: Fabry Disease and the brain #1
b. episode 7: Fabry Disease and the brain #2
C-ANPROM/BE/FAB/0053 - February 2024
Take Care of Rare
Fabry disease and the kidney #2
In this episode Dr. Wim Terryn and Dr. Gert De Schoenmakere are zooming in on the screening process itself and the best techniques to test a suspicious case. When a patient has been diagnosed it is key to test the rest of the family. Can you do it yourself or do you need to refer your patient to a reference center?
Interested in knowing more? Listen to this podcast!
C-ANPROM/BE/FAB/0051 – November 2023
C-ANPROM/BE/FAB/0047