Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP) Syndrome: A Case Report
Journal of Korean Medical Science
;
: 907-910, 2004.
Article
in English
| WPRIM
| ID: wpr-175762
ABSTRACT
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly, childhood-onset noninflammatory arthropathy associated with synovial hyperplasia. Some patients have pro-gressive coxa vara deformity and/or noninflammatory pericardial effusion. CACP is inherited as an autosomal recessive mode and the disease gene is assigned to a 1.9-cM interval on human chromosome 1q25-31. We describe a 10-yr-old boy who has typical features of CACP without familial association.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pericarditis
/
Syndrome
/
Toes
/
Fingers
/
Hip Joint
/
Joint Diseases
Limits:
Adolescent
/
Humans
/
Male
Language:
English
Journal:
Journal of Korean Medical Science
Year:
2004
Type:
Article
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