Beyond Osteogenesis Imperfecta: Causes of Fractures During Infancy and Childhood

被引:8
作者
Bronicki, Lucas M. [1 ]
Stevenson, Roger E. [1 ]
Spranger, Juergen W. [1 ,2 ]
机构
[1] Greenwood Genet Ctr, Greenwood, SC 29646 USA
[2] Johannes Gutenberg Univ Mainz, Childrens Hosp, Mainz, Germany
关键词
skeletal dysplasias; fractures; osteopenia; osteosclerosis; bone fragility; EHLERS-DANLOS-SYNDROME; AKINESIA DEFORMATION SEQUENCE; GAUCHER-DISEASE; SKULL FRACTURES; MUTATIONS; GENE; OSTEOPETROSIS; DERMATOSPARAXIS; OSTEOPOROSIS; GROWTH;
D O I
10.1002/ajmg.c.31466
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fractures in infancy or early childhood require prompt evaluation with consideration of accidental or nonaccidental 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, andmolecular 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. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:314 / 327
页数:14
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