The Recordati Rare Disease Foundation supports the 1st Patient & Expert Meet in Prague on Rare Disease Day, 29th February 2016. The Patient & Expert Meet will bring together key stakeholders, such as patients, clinicians and researchers, from across the world to help increase awareness and improve education about homocystinuria, methylation defects and folate defects. The main goal of the meet is to promote improved health outcomes for patients affected by these disorders.

If you would like a copy of the Recordati Rare Diseases press release you can download it here.

Or alternatively, if you would like to read a copy online, please click here.