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Published in: Calcified Tissue International 6/2015

01-06-2015 | Case Reports

Idiopathic Juvenile Osteoporosis: Clinical Experience from a Single Centre and Screening of LRP5 and LRP6 Genes

Authors: Roberto Franceschi, Monica Vincenzi, Marta Camilot, Franco Antoniazzi, Anthony J. Freemont, Judith E. Adams, Christine Laine, Outi Makitie, M. Zulf Mughal

Published in: Calcified Tissue International | Issue 6/2015

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Abstract

We report clinical findings, bone mineral density (BMD) and bone biopsy data in ten children with features of classic idiopathic juvenile osteoporosis (IJO). We also screened the patients for mutations in LRP5 and LRP6. We found low BMD in the lumbar spine, the hip and distal radius. In the spine and distal radius, the reduction in BMD was more marked in the trabecular compartment. Biopsy confirmed that the trabecular compartment is more severely involved with reduction in bone formation and increase in bone resorption. No mutations in LRP5 and LRP6 could be identified. IJO is likely to be a heterogeneous bone disorder, and next-generation genomic sequencing studies may help reveal causative genes.
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Metadata
Title
Idiopathic Juvenile Osteoporosis: Clinical Experience from a Single Centre and Screening of LRP5 and LRP6 Genes
Authors
Roberto Franceschi
Monica Vincenzi
Marta Camilot
Franco Antoniazzi
Anthony J. Freemont
Judith E. Adams
Christine Laine
Outi Makitie
M. Zulf Mughal
Publication date
01-06-2015
Publisher
Springer US
Published in
Calcified Tissue International / Issue 6/2015
Print ISSN: 0171-967X
Electronic ISSN: 1432-0827
DOI
https://doi.org/10.1007/s00223-015-9983-7

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