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Article

Osteogenesis imperfecta in adults: phenotypic characteristics and response to treatment in an Irish cohort.

Irish journal of medical science - 1 Jun 2014

O'Sullivan E S, van der Kamp S, Kilbane M, McKenna M

Abstract excerpt

BACKGROUND: Osteogenesis imperfecta (OI) is a heritable disorder of variable phenotype that is characterised by bone fragility and frequent fractures, with deformities and short stature in more severe cases. AIMS: We sought to review the response to treatment in a cohort of adult patients with OI...

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Identifiers

PMID: 23918528
DOI: 10.1007/s11845-013-0995-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23918528-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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