I型牙本质发育异常：一个家族中的五例病例。
Dentin dysplasia type I: five cases within one family.
作者信息
Kalk W W, Batenburg R H, Vissink A
机构信息
Department of Oral and Maxillofacial Surgery, University Hospital, Groningen, The Netherlands.
出版信息
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1998 Aug;86(2):175-8. doi: 10.1016/s1079-2104(98)90121-4.
Five cases of dentin dysplasia type I within one family are described. Clinically and radiologically, such patients are characterized by a delayed eruption pattern, opacity of the incisional margins, hypermobility of the teeth, short and defective roots, and obliterated pulp chambers. A conservative attitude toward the treatment of common conditions in dentin dysplasia type I favors the preservation of a vulnerable dentition.
本文描述了一个家族中的5例I型牙本质发育异常病例。从临床和放射学角度来看，这类患者的特征为萌出延迟、切缘不透明、牙齿松动、牙根短且发育不良以及髓腔闭塞。对于I型牙本质发育异常常见病症的治疗采取保守态度有助于保留脆弱的牙列。
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