The CHARGE Syndrome Clinical Database Project (CSCDP) is an internet-based questionnaire designed to collect clinical data on individuals with CHARGE syndrome (CS). Our aims are to: collect information on people with CS of all ages from all over the world, use the collected data to understand more about CS and how it affects different […]
The Scientific Advisory Board (SAB) was established in 2011 to serve as a resource to assist in the identification, funding, and development of scientific research projects. The formation of this new advisory board demonstrates the Foundation’s commitment to investing in high quality scientific research. The SAB consist of leading scientists and medical doctors with extensive research […]
The CHARGE Syndrome Foundation is approaching one million dollars in research grants. 2018 grant applications for scientific and clinical research are now available. CHARGE Syndrome Foundation Scientific Research Grant Program The CHARGE Syndrome Foundation, Inc. announces the availability of scientific research grants of up to $50,000 each. The purpose of these grants is to promote: […]
HOW TO PARTICIPATE IN CHARGE SYNDROME RESEARCH CHARGE research could not take place without the participation of the families. There are many ways you can help. At any given time, there are many studies underway all over the world to help further understand many aspects of CHARGE and CHD7. Studies range from DNA analysis to […]
CHARGE research and CHD7 research help us understand the syndrome, its features and management. Want to participate in research? See Opportunities for Families and start with CSCDP. Check back often to see if new studies have been posted. Looking for grant opportunities? See the RFP information in Foundation Supported Research. Are you a young professional […]
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