Suppr超能文献

Familial odontoid hypoplasia.

作者信息

Stevens Cathy A, Pearce Richard G, Burton Edward M

机构信息

Department of Pediatrics, University of Tennessee College of Medicine, Chattanooga, Tennessee, USA.

出版信息

Am J Med Genet A. 2009 Jun;149A(6):1290-2. doi: 10.1002/ajmg.a.32860.

Abstract

Odontoid hypoplasia is a developmental abnormality, which is often asymptomatic. However significant sequelae can occur in some individuals, particularly after head or neck trauma. This anomaly is not generally known to be familial. We report on four affected individuals in the same family with odontoid hypoplasia, suggesting autosomal dominant inheritance. This is an important observation in that evaluation of family members is warranted in order to identify those at risk of neurologic compromise.

摘要

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验