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 CHARGE Syndrome Foundation is dedicated to promoting high quality clinical and scientific research into the cause and treatment of CHARGE syndrome. We have come a long way over the past couple of years, but know there is way more to be done. CHARGE Syndrome Foundation Scientific Research Grant Program The CHARGE Syndrome Foundation, Inc. […]
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 […]
To learn about the Institute on Movement Studies for Individuals with Visual Impairment or Deafblindness connection to the Foundation watch this video. Canadian scientists in the laboratory of Dr. Nicolas Pilon have found a new gene, Fam172a, that might be involved in CHARGE syndrome. The research “Dysregulation of cotranscriptional […]
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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