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A rare association of osteogenesis imperfecta and juvenile idiopathic arthritis: case reports and li...

A rare association of osteogenesis imperfecta and juvenile idiopathic arthritis: case reports and li...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d96ddd21e941438d96bc44f28f25a4ad

A rare association of osteogenesis imperfecta and juvenile idiopathic arthritis: case reports and literature review

About this item

Full title

A rare association of osteogenesis imperfecta and juvenile idiopathic arthritis: case reports and literature review

Publisher

Hacettepe University Institute of Child Health

Journal title

Turkish journal of pediatrics, 2025-02, p.1-9

Language

English

Formats

Publication information

Publisher

Hacettepe University Institute of Child Health

More information

Scope and Contents

Contents

Background. Osteogenesis imperfecta (OI) is a genetic disorder of connective tissues caused by an abnormality in the synthesis or processing of type I collagen. The combination of OI and inflammatory arthritis is rare. Our literature review identified 5 cases of OI-related inflammatory arthritis, but only 2 of these cases have been reported in chil...

Alternative Titles

Full title

A rare association of osteogenesis imperfecta and juvenile idiopathic arthritis: case reports and literature review

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_d96ddd21e941438d96bc44f28f25a4ad

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d96ddd21e941438d96bc44f28f25a4ad

Other Identifiers

ISSN

0041-4301

E-ISSN

2791-6421

DOI

10.24953/turkjpediatr.2025.5382

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