Juvenile idiopathic arthritis or skeletal dysplasia: first case report of camptodactyly-arthropathy-coxa vara-pericarditis from Iran

Abstract Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome is an inherited autosomal recessive disorder resulting from a mutation in the PRG4 gene located on chromosome one. This mutation leads to either a deficiency or dysfunction of a glycoprotein known as lubricin, which plays a cr...

Full description

Bibliographic Details
Published in:BMC Musculoskeletal Disorders
Main Authors: Niloofar Shashaani, Vadood Javadi, Khosro Rahmani, Reza Shiari
Format: Article
Language:English
Published: BMC 2025-08-01
Subjects:
Camptodactyly
Pericarditis
Children
Skeletal dysplasia
Arthritis
Online Access:https://doi.org/10.1186/s12891-025-09069-x

Internet

https://doi.org/10.1186/s12891-025-09069-x

Similar Items