Suppr超能文献

部分12号染色体短臂缺失:一种导致智力发育迟缓、多种先天性异常综合征的病因。

Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome.

作者信息

Magnelli N C, Therman E

出版信息

J Med Genet. 1975 Mar;12(1):105-8. doi: 10.1136/jmg.12.1.105.

Abstract

A severely mentally retarded man displayed the following main symptoms: short stature, microcephaly, antimongoloid slant of palpebral fissures, big ears with hyperplastic helices, imperfect dental enamel, short and webbed neck, short arms, short hands, brachymetaphalangy, short second fingers, broad thumbs, short metatarsal bones, and unusually big first toes. It seems almost certain that the syndrome was caused by a chromosome deletion involving about half of 12p which was present in all of the lymphocytes examined.

摘要

一名重度智力发育迟缓男子表现出以下主要症状

身材矮小、小头畸形、睑裂反蒙古样倾斜、耳朵大且耳轮增生、牙釉质发育不全、颈部短且有蹼、手臂短、手部短、掌骨短、第二指短、拇指宽、跖骨短以及第一趾异常大。几乎可以确定,该综合征是由涉及12号染色体短臂约一半区域的染色体缺失引起的,在所检测的所有淋巴细胞中均存在这种缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af91/1013240/49f278cdd706/jmedgene00314-0109-a.jpg

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