Catch up on the latest European Registry on Cushing’s Syndrome activities
In 2006, a number of leading European endocrinologists teamed up to apply to the European Union Public Health Programme and succeeded in getting funding for three years (2007-2010). This was used to set up the European Registry on Cushing’s Syndrome. Now, almost 15 years later, the data of more than 2100 patients (as of May 2021) have been included in the database, representing a network of 60 specialist centres in 29 countries and an invaluable resource to help develop research and extended insights into Cushing’s syndrome.
Learn more at ERCUSYN – The European Register on Cushing's Syndrome