Suppr超能文献

5q部分重复综合征:核型相同的两姐妹的表型相似性(5q33部分重复导致5q末端,8p23部分缺失导致p末端)。

Partial duplication 5q syndrome: phenotypic similarity in two sisters with identical karyotype (partial duplication 5q33 leads to 5qter and partial deficiency 8p23 leads to pter).

作者信息

Bartsch-Sandhoff M, Liersch R

出版信息

Ann Genet. 1977 Dec;20(4):281-4.

PMID:305758
Abstract

Two sisters with statomotor developmental retardation microcephaly, hydrocephalus internus and externus without signs of pressure, heart defect (ventricular septal defect), early pulmonary resistance and characteristic facial changes were found to have the same unbalanced karyotype with partial trisomy 5q3300 leads to 5qter and partial monosomy 8p2300 leads to 8pter, derived from a balanced reciprocal paternal translocation: 46,XY,t(5;8)(q3300;p2300). The older girl was tested for the erythrocyte enzyme glutathion reductase. She had normal values.

摘要

发现两名患有静态运动发育迟缓、小头畸形、无颅内压迹象的内外部脑积水、心脏缺陷(室间隔缺损)、早期肺阻力及特征性面部改变的姐妹具有相同的不平衡核型,即5q3300至5qter的部分三体性和8p2300至8pter的部分单体性,源自父亲的平衡相互易位:46,XY,t(5;8)(q3300;p2300)。对年长女孩进行了红细胞酶谷胱甘肽还原酶检测,其值正常。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验