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Axial involvement with facet joint arthropathy and bony ankylosis in a case of camptodactyly, arthropathy, coxa vara, pericarditis (CACP) syndrome.

Abstract：

:Familial arthropathy associated with congenital camptodactyly has been previously recognized as a definite clinical entity in the literature. The clinical spectrum of this disease seems to be variable. The typical features of congenital camptodactyly, arthropathy, coxa vara and pericarditis (CACP syndrome) appear to be a more frequent presentation in children from the Middle East and North Africa. Musculoskeletal presentation of this rare familial form of arthropathy is unique and heterogeneous. In all previous reports, non-inflammatory pattern of arthropathy involving the peripheral joints with typical coxa vara deformity were described, and in a few cases spine abnormalities, including kyphosis, lordosis, or scoliosis. We describe the first case of axial involvement in a typical case of CACP syndrome with facet joint arthropathy and ankylosis at L5/S1 levels.

journal_name

Joint Bone Spine

journal_title

Joint bone spine

authors

Emad Y,Ragab Y,Khalifa M,Bassyouni I,El-Shaarawy N,Rasker JJ

doi

10.1016/j.jbspin.2013.01.010

subject

Has Abstract

pub_date

2013-10-01 00:00:00

pages

520-2

issue

5

eissn

1297-319X

issn

1778-7254

pii

S1297-319X(13)00043-2

journal_volume

80

pub_type

杂志文章

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