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Dentine dysplasia with sclerotic bone and skeletal anomalies inherited as an autosomal dominant trait. A new syndrome.

作者信息

Morris M E, Augsburger R H

出版信息

Oral Surg Oral Med Oral Pathol. 1977 Feb;43(2):267-83. doi: 10.1016/0030-4220(77)90163-3.

DOI:10.1016/0030-4220(77)90163-3
PMID:264650
Abstract

Patients with teeth showing all of the clinical, radiographic, and histologic features of radicular dentine dysplasia (type I) have been found to have dense sclerotic bone and skeletal anomalies of the wrists and hand bones. The association of these defects of teeth and bone was found to be transmitted as an autosomal dominant trait over four generations. Review of theliterature failed to disclose a previous description of this disorder.

摘要

相似文献

1
Dentine dysplasia with sclerotic bone and skeletal anomalies inherited as an autosomal dominant trait. A new syndrome.
Oral Surg Oral Med Oral Pathol. 1977 Feb;43(2):267-83. doi: 10.1016/0030-4220(77)90163-3.
2
Distal osteosclerosis.远端骨硬化
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Dentin dysplasia, type II: a rare autosomal dominant disorder.牙本质发育异常II型:一种罕见的常染色体显性疾病。
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