Cure Sanfilippo Foundation seeks to support research that fills critical gaps in current knowledge across basic science, clinical care, and translational therapeutics which will ultimately improve the lives of children with Sanfilippo syndrome. Scientist-clinician-patient collaborations are highly encouraged. The Foundation is available to assist in facilitating connections with patients/caregivers to inform projects as needed.
Sanfilippo syndrome (MPS III) is a multisystem metabolic disease with prominent neurodevelopmental and neurodegenerative consequences for affected children. There are currently no treatment options available for this terminal condition but we are working hard with the scientific community to change that!
Deadline to Apply: Submit your Letter of Intent (LOI) using the downloadable form to: Research@nullCureSanfilippoFoundation.org,
For more information on this current funding opportunity and LOI form, we invite you to visit us at:
For additional questions, contact Cara@nullCureSanfilippoFoundation.org.