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Musculoskeletal aspects of prune-belly syndrome. Description and pathogenesis.

作者信息

Loder R T, Guiboux J P, Bloom D A, Hensinger R N

机构信息

Section of Orthopaedic, University of Michigan School of Medicine, Ann Arbor.

出版信息

Am J Dis Child. 1992 Oct;146(10):1224-9. doi: 10.1001/archpedi.1992.02160220110034.

Abstract

OBJECTIVE

To determine the types and prevalence of musculoskeletal involvement in children with prune-belly syndrome, and to analyze the pathogenesis of the syndrome in relationship to the musculoskeletal deformities.

DESIGN

A retrospective review of charts and roentgenograms along with a comprehensive review of 188 cases from the literature.

SETTING

Tertiary care children's hospital.

PARTICIPANTS

Twelve boys treated between 1975 and 1990.

MEASUREMENTS/MAIN RESULTS: The prevalence of musculoskeletal involvement in patients was 45%. The involvement can be congenital (eg, clubfeet, limb deficiencies, teratologic hip dysplasia, and vertebral malformations) or developmental (eg, renal osteodystrophy, scoliosis, and pectus excavatum and/or pectus carinatum). The embryologic characteristics of congenital musculoskeletal problems correlate better with the embryologic theory of the prune-belly syndrome (an aberration of mesenchymal development around 6 weeks of gestation) than with the distal urinary tract obstructive theory.

CONCLUSION

Since children with prune-belly syndrome are now living into adulthood, these musculoskeletal aspects will become important regarding potential morbidity.

摘要

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