Suppr超能文献

由于家族性16;20易位导致的16号染色体部分三体。

Partial trisomy 16 as a result of familial 16;20 translocation.

作者信息

Davison E V, Beesley J R

出版信息

J Med Genet. 1984 Oct;21(5):384-6. doi: 10.1136/jmg.21.5.384.

Abstract

Although trisomy 16 is well recognised in spontaneous abortuses, it is infrequent in livebirths and there is little information about the clinical effects. We report two sibs with partial trisomy 16q resulting in infant death. Both children were severely growth retarded with small elfin faces, prominent foreheads, low set ears, abnormal external genitalia, and intractable diarrhoea.

摘要

虽然16三体在自然流产中很常见,但在活产中很少见,而且关于其临床影响的信息很少。我们报告了两名患有部分16q三体的同胞,导致婴儿死亡。两个孩子均严重生长发育迟缓,面部呈小精灵样,前额突出,耳朵低位,外生殖器异常,并有顽固性腹泻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc7/1049325/47712b4e94df/jmedgene00103-0065-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