Rare Diseases Foundation of Iran was approved as associate member at the International Society for Neonatal Screening
RADOIR’s board of directors had a meeting session with Dr. Namaki, the minister of health on Monday April 15th, 2019 at MOH – Iran to present RADOIR’s 10 year activity report .
Rare Diseases Societies joined greeting session at Rare Diseases Foundation of Iran for the Iranian new year and met with the chairman and the managing director of RADOIR
The Iranian minister of health authorized Tehran Medical University (TUMS) to establish the national strategic plan for rare diseases in cooperation with Rare Diseases Foundation of Iran
Researchers at Danish Project iPSYCH & the Broad Institute in USA have found a common genetic risk for autism. The discovery means the determination of genes by separating the diagnosis groups and making more exact diagnoses will be accessible in the future.
A study carried out by iPSYCH shows that particular genetic variants in the human genome that are important for the development of the brain early in the life of the fetus are frequently found in psychiatric disorders.