Literature DB >> 26531771

Beyond osteogenesis imperfecta: Causes of fractures during infancy and childhood.

Lucas M Bronicki, Roger E Stevenson, Jürgen W Spranger.   

Abstract

Fractures in infancy or early childhood require prompt evaluation with consideration of accidental or non-accidental trauma as well as a large number of genetic disorders that predispose to fractures. Bone fragility has been reported in more than 100 genetic disorders, including skeletal dysplasias, inborn errors of metabolism and congenital insensitivity to pain. Most of these disorders are rare but often have distinctive clinical or radiographic findings to assist in the diagnosis. Gene sequencing is available, albeit connective tissue and skeletal dysplasia panels and biochemical studies are only helpful in a minority of cases. This article presents the clinical, radiographic, and molecular profiles of the most common heritable disorders other than osteogenesis imperfecta with increased bone fragility. In addition, the clinicians must consider non-heritable influences such as extreme prematurity, prenatal viral infection and neoplasia in the diagnostic process.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  bone fragility; fractures; osteopenia; osteosclerosis; skeletal dysplasias

Mesh:

Year:  2015        PMID: 26531771     DOI: 10.1002/ajmg.c.31466

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  6 in total

Review 1.  Osteogenesis imperfecta in children and adolescents-new developments in diagnosis and treatment.

Authors:  P Trejo; F Rauch
Journal:  Osteoporos Int       Date:  2016-08-05       Impact factor: 4.507

Review 2.  Ehlers-Danlos syndrome: what the radiologist needs to know.

Authors:  Michael P George; Natasha E Shur; Jeannette M Peréz-Rosselló
Journal:  Pediatr Radiol       Date:  2021-05-17

Review 3.  The biology of bone lengthening.

Authors:  Ivan Hvid; Joachim Horn; Stefan Huhnstock; Harald Steen
Journal:  J Child Orthop       Date:  2016-11-12       Impact factor: 1.548

4.  An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes.

Authors:  Polona Le Quesne Stabej; Chela James; Louise Ocaka; Mehmet Tekman; Stephanie Grunewald; Emma Clement; Horia C Stanescu; Robert Kleta; Deborah Morrogh; Alistair Calder; Hywel J Williams; Maria Bitner-Glindzicz
Journal:  Orphanet J Rare Dis       Date:  2017-02-07       Impact factor: 4.123

5.  Revisiting the radiographic assessment of osteoporosis-Osteopenia in children 0-2 years of age. A systematic review.

Authors:  Karen Rosendahl; Anette Lundestad; John Asle Bjørlykke; Regina Küfner Lein; Oskar Angenete; Thomas Angell Augdal; Lil-Sofie Ording Müller; Diego Jaramillo
Journal:  PLoS One       Date:  2020-11-02       Impact factor: 3.240

6.  Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing.

Authors:  Harvy Mauricio Velasco; Jessica L Morales
Journal:  Appl Clin Genet       Date:  2017-11-07
  6 in total

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