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Article

A rare case of osteogenesis imperfecta combined with complete tooth loss.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Jan 2014

Lu Yanqin, Zhao Fei, Ren Xiuzhi, Li Zhiliang, Yang Xiaomeng, Han Jinxiang

Abstract excerpt

Osteogenesis imperfecta (OI) is a heritable disorder of the connective tissue characterized by blue sclerae, osteoporosis and bone fragility. Dentinogenesis imperfecta type I is commonly seen in OI patients, but other dental impairments, such as tooth agenesis or complete tooth loss, are rarely reported for these patients. Here, we report the case of a 37-year-old female Chinese OI patient who experienced...

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PMID: 23934635
DOI: 10.1515/jpem-2013-0069

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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