CACP

Camptodactyly-Arthropathy-Coxa vara-Pericarditis (CACP) Syndrome is an autosomal recessive syndrome characterized by flexion contractures of the fingers and/or toes, progressive, non-inflammatory arthropathy of multiple joints, and varus hip alignment. Other names for CACP syndrome have included Arthropathy Camptodactyly Syndrome, Congenital Familial Hypertrophic Synovitis, Jacobs Syndrome, and Familial Fibrosing Serositis. 

The purpose of this website, CACP Connect is to provide information and support to individuals with CACP Syndrome and their families and to promote scientific research to advance the diagnosis and treatment of CACP syndrome and its associated conditions.

For more information, please contact Erin Teeple at Erin_Teeple@brown.edu.