Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP) Syndrome: A Case Report
Journal of Korean Medical Science
;
: 907-910, 2004.
Artículo
en Inglés
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Pericarditis
/
Síndrome
/
Dedos del Pie
/
Dedos
/
Articulación de la Cadera
/
Artropatías
Límite:
Adolescente
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Journal of Korean Medical Science
Año:
2004
Tipo del documento:
Artículo
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