Naseem Amin, CEO of Orphalan, explores Wilson’s disease and current FDA-approved treatments.
Sage Sargent, patient advocate for congenital adrenal hyperplasia, shares her experience as an intersex person with the condition.
Our reflection of the 41st annual National Society of Genetic Counselors conference including favorite sessions and what we learned in Nashville.
Author and law professor, Jorge Contreras, give an overview of his latest novel, The Genome Defense.
Dr. Tristan Hardy provides an overview of reproductive medicine focusing on the relevant aspects of biological family health history.
Dr. Julian Barwell shares insight on the 100,000 Genomes Project and how digital pedigrees are essential to the project and healthcare.
The robust processes to evaluate applications to n-Lorem’s nano-rare patient treatments.
Amber Olsen and Faith McGown of the United MSD Foundation discuss Multiple Sulfatase Deficiency.
Podcast host and rare disease advocate, Effie Parks, chats about her son Ford who has CTNNB1 Syndrome.