White Sutton Syndrome Foundation

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. The mission of the White Sutton Syndrome Foundation is to build a community that will improve the quality of life for those diagnosed with White Sutton Syndrome and their families, to educate others about this condition and to fund research in order to better understand its symptoms, treatments and prognosis. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.