MECP2 Duplication Global

MECP2 Duplication Syndrome is a rare disease caused by a duplication of the MECP2 gene. It is progressive and usually includes neurological, developmental, gastrointestinal, pulmonary, and musculoskeletal symptoms. The mission of MDG is to unite advocacy groups worldwide to accelerate research, improve care, and raise awareness of MECP2 Duplication Syndrome.