[Syndromes 16. Osteogenesis imperfecta].
作者信息
Vissink A, Hoff M, Stolte-Dijkstra I, Bergman K A
机构信息
Kliniek voor Mondziekten, Kaakchirurgie en Bijzondere Tandheelkunde, Academisch Ziekenhuis Groningen, Postbus 30.001, 9700 RB Groningen.
出版信息
Ned Tijdschr Tandheelkd. 1999 Dec;106(12):454-7.
PMID:11930846
Abstract
Osteogenesis imperfecta consists of a group of hereditary connective tissue diseases with fragility of the bone as a general feature. Frequently occurring other characteristics are blue sclerae, opalescent teeth, hearing loss, disorders of the skeleton, and hyperextensibility of the joints. Obliteration and the unusual shape of the pulp chambers may interfere with dental treatment.
摘要
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