This investigation examined the validity of the hypothesis that the acetabulum in congenital
1. Complete rupture of the axillary artery caused by
1. The lesions chiefly responsible for persistent pain and weakness after acromio-clavicular
We have reviewed 30 patients who had been treated conservatively for acromioclavicular
Recurrent
Drawing upon a total experience of 450 hips affected by established congenital
1. Fifty cases of recurrent
1. The combination of femoral shaft fracture with
We report nine cases of irreducible congenital
A new technique for repair of neglected posterior
A retrospective survey of 135 posterior
1. A case is reported of traumatic
Computerised arthrotomography was performed on 33 patients four to six weeks after acute primary anterior
Congenital
From 1956 to 1965, congenital
We report a review of 33 hips (32 patients) which had required repeat open reduction for congenital
Between 1956 1999, 132 601 living children were born in and Malmö, and screened for neonatal instability of the hip. All late diagnosed patients have been followed and re-examined clinically and radiologically. During the first years of screening, less than five per 1000 living newborn infants were treated. This figure increased to 35 per 1000 in 1980, but later diminished again to about six per 1000 annually after 1990. The number of referred cases decreased from 45 per 1000 in 1980 to between 10 to 15 per 1000 from 1990. During the period of high rates of referral and treatment a larger number of paediatricians were involved in the screening procedure than during the periods with low rates of referral and treatment. Altogether 21 patients (0.16 per 1000) with developmental
1. In unreduced congenital
1. A simple test more sensitive than Ortolani's for the diagnosis of instability of the hip in the new-born is described. It takes only a few seconds to perform and can be quickly taught to doctors, nurses and midwives. 2. About one infant in sixty is born with instability of one or both hips. Over 60 per cent of these recover in the first week of life, and 88 per cent in the first two months. The remaining 12 per cent are true congenital
After