Literature DB >> 2766569

Osteogenesis imperfecta with congenital joint contractures (Bruck syndrome).

D Viljoen1, G Versfeld, P Beighton.   

Abstract

Five children from three unrelated families were born with symmetrical contractures of the knees, ankles and feet. An initial diagnosis of arthrogryposis multiplex was made, but frequent fracturing occurred after walking commenced and it was then recognised that the children had osteogenesis imperfecta. The pathogenesis of the congenital contractures is unknown, but the symmetry and lack of evidence of prior fracturing is suggestive of articular immobility during early intra-uterine development. The consistency of the anatomical distribution of the contractures, in the setting of a uniform OI phenotype, is suggestive of syndromic identity. A similar case was documented by Alfred Bruck in 1897 and we propose that the eponymous designation "Bruck syndrome" should be applied to the disorder.

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Year:  1989        PMID: 2766569     DOI: 10.1111/j.1399-0004.1989.tb03174.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  18 in total

1.  FKBP10 and Bruck syndrome: phenotypic heterogeneity or call for reclassification?

Authors:  Ranad Shaheen; Mohammed Al-Owain; Nadia Sakati; Zayed S Alzayed; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2010-08-13       Impact factor: 11.025

Review 2.  International classification of osteochondrodysplasias. The International Working Group on Constitutional Diseases of Bone.

Authors:  J Spranger
Journal:  Eur J Pediatr       Date:  1992-06       Impact factor: 3.183

3.  Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17.

Authors:  R A Bank; S P Robins; C Wijmenga; L J Breslau-Siderius; A F Bardoel; H A van der Sluijs; H E Pruijs; J M TeKoppele
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-02       Impact factor: 11.205

4.  Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3.

Authors:  Muhammad Umair; Bader Alhaddad; Afzal Rafique; Abid Jan; Tobias B Haack; Elisabeth Graf; Asmat Ullah; Farooq Ahmad; Tim M Strom; Thomas Meitinger; Wasim Ahmad
Journal:  Pediatr Res       Date:  2017-07-26       Impact factor: 3.756

5.  Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta.

Authors:  Lutz Garbes; Kyungho Kim; Angelika Rieß; Heike Hoyer-Kuhn; Filippo Beleggia; Andrea Bevot; Mi Jeong Kim; Yang Hoon Huh; Hee-Seok Kweon; Ravi Savarirayan; David Amor; Purvi M Kakadia; Tobias Lindig; Karl Oliver Kagan; Jutta Becker; Simeon A Boyadjiev; Bernd Wollnik; Oliver Semler; Stefan K Bohlander; Jinoh Kim; Christian Netzer
Journal:  Am J Hum Genet       Date:  2015-02-12       Impact factor: 11.025

6.  Defective collagen fibril formation and mineralization in osteogenesis imperfecta with congenital joint contractures (Bruck syndrome).

Authors:  R E Brenner; U Vetter; H Stöss; P K Müller; W M Teller
Journal:  Eur J Pediatr       Date:  1993-06       Impact factor: 3.183

7.  Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen.

Authors:  Ulrike Schwarze; Tim Cundy; Shawna M Pyott; Helena E Christiansen; Madhuri R Hegde; Ruud A Bank; Gerard Pals; Arunkanth Ankala; Karen Conneely; Laurie Seaver; Suzanne M Yandow; Ellen Raney; Dusica Babovic-Vuksanovic; Joan Stoler; Ziva Ben-Neriah; Reeval Segel; Sari Lieberman; Liesbeth Siderius; Aida Al-Aqeel; Mark Hannibal; Louanne Hudgins; Elizabeth McPherson; Michele Clemens; Michael D Sussman; Robert D Steiner; John Mahan; Rosemarie Smith; Kwame Anyane-Yeboa; Julia Wynn; Karen Chong; Tami Uster; Salim Aftimos; V Reid Sutton; Elaine C Davis; Lammy S Kim; Mary Ann Weis; David Eyre; Peter H Byers
Journal:  Hum Mol Genet       Date:  2012-09-04       Impact factor: 6.150

8.  Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome.

Authors:  Brian P Kelley; Fransiska Malfait; Luisa Bonafe; Dustin Baldridge; Erica Homan; Sofie Symoens; Andy Willaert; Nursel Elcioglu; Lionel Van Maldergem; Christine Verellen-Dumoulin; Yves Gillerot; Dobrawa Napierala; Deborah Krakow; Peter Beighton; Andrea Superti-Furga; Anne De Paepe; Brendan Lee
Journal:  J Bone Miner Res       Date:  2011-03       Impact factor: 6.741

9.  Osteogenesis imperfecta type V, spot diagnosis.

Authors:  Kazimierz Kozlowski
Journal:  Pol J Radiol       Date:  2010-01

Review 10.  Syndromes with congenital brittle bones.

Authors:  Horacio Plotkin
Journal:  BMC Pediatr       Date:  2004-08-31       Impact factor: 2.125

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