Diagnostic Challenges in Bone Fragility: Osteogenesis Imperfecta Case Series

Diagnostic Challenges in Bone Fragility: Osteogenesis Imperfecta Case Series

Osteogenesis imperfecta (OI) is a rare hereditary connective tissue disorder. Diagnosis is typically clinical; genetic testing can contribute. <b>Objectives</b>: We are presenting a case series of type I OI in Romanian patients, showcasing the difficulties in diagnostic and case manageme...

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Bibliographic Details
Main Authors: Andrei Costache, Anca-Lelia Riza, Mihaela Popescu, Rebecca-Cristiana Șerban, Andreea-Mădălina Mituț-Velișcu, Ioana Streață
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Biomedicines
Subjects:
osteogenesis imperfecta
connective tissue disorder
genetic testing
case series
Online Access:https://www.mdpi.com/2227-9059/13/4/865
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