Pelvic dysplasia associated with arthrogrypotic changes in the lower extremities. A new syndrome.

Abstract:

:Two sisters exhibit arthrogrypotic changes in the lower extremities associated with a previously undescribed pelvic dysplasia. The pelvic dysplasia is characterized by: severe abnormalities of ossification with markedly widened triradiate cartilages; irregular, notched acetabulae; marked hypoplasia of the ilia; notching of the iliac wings; and delayed ossification of the capital femoral ossific nucleus. The elder girl has bilateral clubfeet, as well as flexion contractures of both knees. The younger girl has a right talipes equinovarus and left hip dislocation. Autosomal recessive inheritance is suggested. This distinctive syndrome should be considered in the differential diagnosis of the patient with arthrogryposis.

journal_name

Clin Orthop Relat Res

authors

Ray S,Peterson PD,Scott CI Jr

subject

Has Abstract

pub_date

1986-06-01 00:00:00

pages

99-102

issue

207

eissn

0009-921X

issn

1528-1132

pub_type

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