Association for Creatine Deficiencies

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. Our mission is to provide support and education to families and the scientific community, advocate for early diagnoses through newborn screening, and support and fund research for treatments and cures for Cerebral Creatine Deficiency Syndromes (CCDS) including AGAT Deficiency, GAMT Deficiency, and Creatine Transporter Deficiency (CTD). Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.