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01-01-2016 | Review

Bone impairment in primary hyperoxaluria: a review

Authors: Justine Bacchetta, Georges Boivin, Pierre Cochat

Published in: Pediatric Nephrology | Issue 1/2016

Abstract

Deposition of calcium oxalate crystals in the kidney and bone is a hallmark of primary hyperoxaluria (PH). Since the bone compartment can store massive amounts of oxalate, patients present with recurrent low-trauma fractures, bone deformations, severe bone pains, and specific oxalate osteopathy on X-ray. Bone biopsy from the iliac crest displays specific features such as oxalate crystals surrounded by a granulomatous reaction corresponding to an invasion of bone surface by macrophages. The objective of this manuscript is therefore to provide an overview of bone impairment in PH, by reviewing the current literature on bone and dental symptoms as well as imaging techniques used for assessing bone disease.

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Title: Bone impairment in primary hyperoxaluria: a review
Authors: Justine Bacchetta
Georges Boivin
Pierre Cochat
Publication date: 01-01-2016
Publisher: Springer Berlin Heidelberg
Published in: Pediatric Nephrology / Issue 1/2016
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI: https://doi.org/10.1007/s00467-015-3048-z

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Springer Medicine

Bone impairment in primary hyperoxaluria: a review

Abstract

Keynote webinar | Spotlight on medication adherence

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