Literature DB >> 12151877

Advances in osteogenesis imperfecta.

William G Cole1.   

Abstract

Considerable progress has been made in many aspects of osteogenesis imperfecta. The international Sillence classification of osteogenesis imperfecta is being expanded to include a greater range of subgroups of patients. Attempts are being made to identify the genes causing forms of osteogenesis imperfecta and related syndromes that are not caused by mutations of the Type I collagen genes. In medium-term studies, bisphosphonate treatment has been shown to be the first method of treatment to improve the clinical course of the disease significantly. Somatic cell therapy, using allogeneic bone marrow and mesenchymal stromal cell transplantation, are in their early phases of development for use in humans with osteogenesis imperfecta. Somatic gene therapy, which aims to inactivate the mutation, is being evaluated in laboratory and animal studies.

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Year:  2002        PMID: 12151877     DOI: 10.1097/00003086-200208000-00003

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  9 in total

Review 1.  Genetic disorders of the skeleton: a developmental approach.

Authors:  Uwe Kornak; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2003-07-31       Impact factor: 11.025

2.  Case report: osteogenesis imperfecta Elusive cause of fractures.

Authors:  Elizabeth L Strevel; Alexandra Papaioannou; Jonathan D Adachi; Marty McNamara
Journal:  Can Fam Physician       Date:  2005-12       Impact factor: 3.275

3.  A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.

Authors:  Robert C Gensure; Outi Mäkitie; Catherine Barclay; Catherine Chan; Steven R Depalma; Murat Bastepe; Hilal Abuzahra; Richard Couper; Stefan Mundlos; David Sillence; Leena Ala Kokko; Jonathan G Seidman; William G Cole; Harald Jüppner
Journal:  J Clin Invest       Date:  2005-05       Impact factor: 14.808

Review 4.  Bisphosphonate therapy for osteogenesis imperfecta.

Authors:  Kerry Dwan; Carrie A Phillipi; Robert D Steiner; Donald Basel
Journal:  Cochrane Database Syst Rev       Date:  2016-10-19

5.  How tough is brittle bone? Investigating osteogenesis imperfecta in mouse bone.

Authors:  R O Ritchie; S J Shefelbine; A Carriero; E A Zimmermann; A Paluszny; S Y Tang; H Bale; B Busse; T Alliston; G Kazakia
Journal:  J Bone Miner Res       Date:  2014-06       Impact factor: 6.741

6.  The Use of Patient-Specific Induced Pluripotent Stem Cells (iPSCs) to Identify Osteoclast Defects in Rare Genetic Bone Disorders.

Authors:  I-Ping Chen
Journal:  J Clin Med       Date:  2014-12-17       Impact factor: 4.241

7.  Health-related quality of life of children and adolescents with osteogenesis imperfecta: a cross-sectional study using PedsQL™.

Authors:  Ana Paula Vanz; Juliana van de Sande Lee; Bruna Pinheiro; Marina Zambrano; Evelise Brizola; Neusa Sicca da Rocha; Ida Vanessa D Schwartz; Maria Marlene de Souza Pires; Têmis Maria Félix
Journal:  BMC Pediatr       Date:  2018-03-02       Impact factor: 2.125

8.  Brittle teeth with brittle bone in a family for four generations: Case report and literature review.

Authors:  P S Shilpa; Chaya M David; Rachna Kaul; C J Sanjay; B K Ram Narayan
Journal:  Contemp Clin Dent       Date:  2012-04

9.  ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.

Authors:  Thomas S Lisse; Frank Thiele; Helmut Fuchs; Wolfgang Hans; Gerhard K H Przemeck; Koichiro Abe; Birgit Rathkolb; Leticia Quintanilla-Martinez; Gabriele Hoelzlwimmer; Miep Helfrich; Eckhard Wolf; Stuart H Ralston; Martin Hrabé de Angelis
Journal:  PLoS Genet       Date:  2008-02       Impact factor: 5.917

  9 in total

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