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Additional findings can include synkinesia of the digits, unilateral renal agenesis, sensorineural hearing loss, cleft lip and/or palate, agenesis of one or more teeth, brachydactyly, syndactyly, and agenesis of the corpus callosum.

其他表现可包括手指联带运动、单侧肾脏发育不全、感音性听力丧失、裂唇和/或裂腭、一个或多个牙齿发育不全、短指、并指以及胼胝体发育不全。

Uni- or bilateral radial ray malformation including thenar hypoplasia, thumb hypoplasia/aplasia, triphalangeal, preaxial polydactyly, clubhand, deviation of the forearms, Duane anomaly, sensorineural or conductive deafness, and renal abnormalities

单侧或双侧桡骨线变形包括手掌发育不良,拇指发育不良/发育不全,三指节畸形,轴前并指畸形,畸形手,前臂偏斜,Duane异常,感觉神经性或传导性耳聋,和肾的异常。

Father Conmee gave a letter from his breast to Master Brunny Lynam and pointed to the red pillarbox at the corner of Fitzgibbon street.

14康米神父从前胸掏出一封信来,递给少年布鲁尼。莱纳姆,并指了指菲茨吉本街拐角处的红色邮筒。

I nudge her and pointed to the man across the street.

我用肘碰了她一下并指了指街对面的那个男的。

Simple syndactyly is more common between the third and fourth fingers and the second and third toes.

简单的并指畸形常发生于第三和第四指以及第二和第三趾之间。50%的病例是双侧发病的。

To observe the effect of frifting fingerweb flap on treating congenital incomplete syndactyly.

目的 观察指蹼皮瓣滑移术治疗先天性不完全性并指畸形的疗效。

Complex syndactyly refers to fingers joined by bone or cartilaginous union, usually in a side-to-side fashion at the distal phalanges.

复合并指畸形表明手指由骨或软骨连接,通常形成在指末端形成并排形式。

Fingerweb flap was frifted to treat 5 cases of congenital incomplete cutaneous syndactyly.

采用指蹼皮瓣滑移术治疗先天性不完全性皮肤性并指畸形5例。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

本研究通过连锁分析和直接测序的方法,分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

中文摘要本研究通过连锁分析和直接测序的方法,分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

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