Angelman syndrome is a rare genetic disorder caused by mutations in the maternally-inherited UBE3A gene and characterized by poor muscle control, limited speech, epilepsy, and intellectual disabilities.
EMA asks for more information after safety signal arises for GLP-1s, semaglutide in thyroid cancer
The European Medicines Agency is concerned there could be a potential link between thyroid cancer and the use of glucagon-like peptide-1 (GLP-1) receptor agonists, which