Literature DB >> 9129737

Bruck syndrome (osteogenesis imperfecta with congenital joint contractures): review and report on the first North American case.

E McPherson1, M Clemens.   

Abstract

We describe a patient who was born with flexion contractures and pterygia at the elbows, clubfeet, torticollis, and several rib fractures. During infancy and childhood, multiple fractures of the lower limbs occurred with minimal trauma and led to disabling deformities. When evaluated at age 19 years, he was normally intelligent, but extremely short, with severe kyphoscoliosis compromising his pulmonary function. Pterygia limited elbow extension to 90 degrees, and severe lower limb deformities prevented ambulation. He did not have blue sclerae, dentinogenesis imperfecta, or hearing loss. X-ray studies showed demineralized bones, severe deformity and cystic change at old fracture sites, and vertebral wedging. Collagen studies on skin fibroblasts were normal.

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Mesh:

Year:  1997        PMID: 9129737

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  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

2.  De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.

Authors:  Charuta Gavankar Furey; Jungmin Choi; Sheng Chih Jin; Xue Zeng; Andrew T Timberlake; Carol Nelson-Williams; M Shahid Mansuri; Qiongshi Lu; Daniel Duran; Shreyas Panchagnula; August Allocco; Jason K Karimy; Arjun Khanna; Jonathan R Gaillard; Tyrone DeSpenza; Prince Antwi; Erin Loring; William E Butler; Edward R Smith; Benjamin C Warf; Jennifer M Strahle; David D Limbrick; Phillip B Storm; Gregory Heuer; Eric M Jackson; Bermans J Iskandar; James M Johnston; Irina Tikhonova; Christopher Castaldi; Francesc López-Giráldez; Robert D Bjornson; James R Knight; Kaya Bilguvar; Shrikant Mane; Seth L Alper; Shozeb Haider; Bulent Guclu; Yasar Bayri; Yener Sahin; Michael L J Apuzzo; Charles C Duncan; Michael L DiLuna; Murat Günel; Richard P Lifton; Kristopher T Kahle
Journal:  Neuron       Date:  2018-07-05       Impact factor: 17.173

Review 3.  The genetic implication of scoliosis in osteogenesis imperfecta: a review.

Authors:  Gang Liu; Jia Chen; Yangzhong Zhou; Yuzhi Zuo; Sen Liu; Weisheng Chen; Zhihong Wu; Nan Wu
Journal:  J Spine Surg       Date:  2017-12

4.  Arthrogryposis multiplex congenita in a child with congenital fractures: a case report.

Authors:  Kavinda Dayasiri; Heshan Jayaweera
Journal:  J Med Case Rep       Date:  2022-10-19

5.  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

6.  Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients.

Authors:  Peiran Zhou; Yi Liu; Fang Lv; Min Nie; Yan Jiang; Ou Wang; Weibo Xia; Xiaoping Xing; Mei Li
Journal:  PLoS One       Date:  2014-09-19       Impact factor: 3.240

7.  Molecular spectrum and differential diagnosis in patients referred with sporadic or autosomal recessive osteogenesis imperfecta.

Authors:  Jose A Caparros-Martin; Mona S Aglan; Samia Temtamy; Ghada A Otaify; Maria Valencia; Julián Nevado; Elena Vallespin; Angela Del Pozo; Carmen Prior de Castro; Lucia Calatrava-Ferreras; Pilar Gutierrez; Ana M Bueno; Belen Sagastizabal; Encarna Guillen-Navarro; Maria Ballesta-Martinez; Vanesa Gonzalez; Sarenur Y Basaran; Ruksan Buyukoglan; Bilge Sarikepe; Cecilia Espinoza-Valdez; Francisco Cammarata-Scalisi; Victor Martinez-Glez; Karen E Heath; Pablo Lapunzina; Victor L Ruiz-Perez
Journal:  Mol Genet Genomic Med       Date:  2016-12-20       Impact factor: 2.183

Review 8.  Syndromes with congenital brittle bones.

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

  8 in total

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