LECTURES: Advances in Diagnostics and Emerging Therapies for Rare Diseases
Tracks
HALL A
| Friday, October 9, 2026 |
| 4:00 PM - 5:20 PM |
Details
Chairs: Mehmet Vural (Turkey), Giuseppe Buonocore (Italy)
16:00 - 16:15
Newborn screening of genetic disorders
Didier Lacombe (France)
16:15 - 16:30
Advances in Recognition, Diagnosis and Management of Lysosomal Storage Disorders
Melike Ersoy (Turkey)
16:30 - 16:45
Familial Hypercholesterolemia: New Horizons for Diagnosis and Effective Management
Lorenzo Iughetti (Italy)
16:45 - 17:00
Designing a comprehensive framework to enhance diagnosis, treatment, and support for children living with rare disease
Ellen Crushell (Ireland)
17:00 - 17:15
Q&A
16:00 - 16:15
Newborn screening of genetic disorders
Didier Lacombe (France)
16:15 - 16:30
Advances in Recognition, Diagnosis and Management of Lysosomal Storage Disorders
Melike Ersoy (Turkey)
16:30 - 16:45
Familial Hypercholesterolemia: New Horizons for Diagnosis and Effective Management
Lorenzo Iughetti (Italy)
16:45 - 17:00
Designing a comprehensive framework to enhance diagnosis, treatment, and support for children living with rare disease
Ellen Crushell (Ireland)
17:00 - 17:15
Q&A
The Organising Secretariat
For any questions or comments, please contact us at info@mcascientificevents.eu
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