Suppr超能文献

纳杰尔肢体颜面发育不全的常染色体隐性遗传。

Autosomal recessive inheritance of Nager acrofacial dysostosis.

作者信息

Chemke J, Mogilner B M, Ben-Itzhak I, Zurkowski L, Ophir D

机构信息

Clinical Genetics Unit, Kaplan Hospital, Rehovot, Israel.

出版信息

J Med Genet. 1988 Apr;25(4):230-2. doi: 10.1136/jmg.25.4.230.

Abstract

Nager acrofacial dysostosis is a variant of mandibulofacial dysostosis with severe micrognathia, malar hypoplasia, and radial limb defects. Most cases are sporadic, but autosomal recessive inheritance has been suggested. A family is reported in which two sibs are affected by this syndrome, presenting further evidence for autosomal recessive inheritance. The recognition of this syndrome as a distinct entity has important implications. After the birth of a child with orofacial malformations suggestive of mandibulofacial dysostosis, an exact diagnosis is essential before genetic counselling can be offered.

摘要

纳杰尔肢端颜面发育不全是下颌面骨发育不全的一种变异型,伴有严重小颌畸形、颧骨发育不全和桡骨肢体缺陷。大多数病例为散发性,但有人提出其为常染色体隐性遗传。本文报道了一个家庭,其中两个同胞患有此综合征,为常染色体隐性遗传提供了进一步证据。将此综合征识别为一个独立的实体具有重要意义。在出生一个有提示下颌面骨发育不全的口面部畸形患儿后,在提供遗传咨询之前,准确诊断至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fd/1015502/258490621255/jmedgene00066-0015-a.jpg

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