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
The referral trajectory
With over 6000 rare diseases, you as specialists often face challenges in identifying their symptoms and consequently offering the best patient care. Prof. Dr. David Cassiman, head of the metabolic center in UZ Leuven, elaborates on the symptoms of Fabry disease and explains which tests to perform in case of suspicion.
How can a reference center in metabolic diseases help you and your patients in this diagnostic odyssey, and which are the treatment options for patients with Fabry disease? Do you wonder what the answers to these questions are? Listen to( t)his podcast!
C-ANPROM/BE/FAB/0051 – November 2023
C-ANPROM/BE/FAB/0045