Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures

E. J. Breslau-Siderius; R. H. Engelbert; G. Pals; J. A. van der Sluijs

doi:10.1097/01202412-199801000-00006

Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures

E. J. Breslau-Siderius
, R. H. Engelbert
, G. Pals
, J. A. van der Sluijs

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

Bruck syndrome manifests with combined features of arthrogryposis and osteogenesis imperfecta. It is a distinct autosomal recessive disorder with normal collagen I. The main features are osteoporosis, bowing of the long bones, scoliosis due to vertebral deformities, and congenital joint contractures. The presence of arthrogryposis differentiates this syndrome from "classical" osteogenesis imperfecta. A family with three affected children is presented with a review of the literature

Original language	English
Pages (from-to)	35-38
Journal	Journal of pediatric orthopaedics. Part B / European Paediatric Orthopaedic Society, Pediatric Orthopaedic Society of North America
Volume	7
Issue number	1
DOIs	https://doi.org/10.1097/01202412-199801000-00006
Publication status	Published - 1998

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Breslau-Siderius, E. J., Engelbert, R. H., Pals, G., & van der Sluijs, J. A. (1998). Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures. Journal of pediatric orthopaedics. Part B / European Paediatric Orthopaedic Society, Pediatric Orthopaedic Society of North America, 7(1), 35-38. https://doi.org/10.1097/01202412-199801000-00006

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abstract = "Bruck syndrome manifests with combined features of arthrogryposis and osteogenesis imperfecta. It is a distinct autosomal recessive disorder with normal collagen I. The main features are osteoporosis, bowing of the long bones, scoliosis due to vertebral deformities, and congenital joint contractures. The presence of arthrogryposis differentiates this syndrome from {"}classical{"} osteogenesis imperfecta. A family with three affected children is presented with a review of the literature",

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Breslau-Siderius, EJ, Engelbert, RH, Pals, G & van der Sluijs, JA 1998, 'Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures', Journal of pediatric orthopaedics. Part B / European Paediatric Orthopaedic Society, Pediatric Orthopaedic Society of North America, vol. 7, no. 1, pp. 35-38. https://doi.org/10.1097/01202412-199801000-00006

Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures. / Breslau-Siderius, E. J.; Engelbert, R. H.; Pals, G. et al.
In: Journal of pediatric orthopaedics. Part B / European Paediatric Orthopaedic Society, Pediatric Orthopaedic Society of North America, Vol. 7, No. 1, 1998, p. 35-38.

Research output: Contribution to journal › Article › Academic › peer-review

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AB - Bruck syndrome manifests with combined features of arthrogryposis and osteogenesis imperfecta. It is a distinct autosomal recessive disorder with normal collagen I. The main features are osteoporosis, bowing of the long bones, scoliosis due to vertebral deformities, and congenital joint contractures. The presence of arthrogryposis differentiates this syndrome from "classical" osteogenesis imperfecta. A family with three affected children is presented with a review of the literature

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Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures

Abstract

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