Suppr超能文献

一种具有脊髓小脑共济失调且可能为常染色体隐性遗传的独特畸形综合征。

A distinct dysmorphic syndrome with spinocerebellar ataxia and probable autosomal recessive inheritance.

作者信息

Sánchez-Corona J, García-Cruz D, González-Angulo A, Alvarez-Arratia M C, Rodríguez R M, Cantú J M

出版信息

Hum Genet. 1985;69(3):243-5. doi: 10.1007/BF00293033.

Abstract

Two brothers and their sister aged 8, 13, and 7 years were found to have unusual facies (gross, rough and abundant hair, wide forehead, mild palpebral ptosis, small nose, anteverted nostrils, thick lips, and down-slanting corners of the mouth), dysarthria, delayed psychomotor development, scoliosis, feet deformities, and limb and gait ataxia. The characteristic clinical picture in the three sibs, once compared with other ataxic syndromes, allowed one to conclude that this could correspond to a distinct entity probably inherited as an autosomal recessive disorder.

摘要

发现两名兄弟及其8岁、13岁和7岁的妹妹有异常面容(面容粗糙、毛发浓密、额头宽阔、轻度上睑下垂、鼻子小、鼻孔前倾、嘴唇厚、嘴角向下倾斜)、构音障碍、精神运动发育迟缓、脊柱侧弯、足部畸形以及肢体和步态共济失调。这三名同胞的特征性临床表现一旦与其他共济失调综合征进行比较,就可以得出结论,这可能对应于一种独特的疾病实体,可能以常染色体隐性疾病的方式遗传。

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