并指畸形

The diagnosis is easier when the syndactyly is complete and complex because it is associated with bony changes in shape and results in synchronous movements of the affected digits.

当并指畸形时完全型和复合型时，诊断相对容易，因为它有骨骼形状的改变，引起受累手指同步运动。

Syndactyly is defined as simple when it involves soft tissue only or complex when it involves the bone or nail of the adjacent fingers or toes that are joined side by side.

简单的并指畸形定义只包括软组织，复合的定义包括连接临近手指或脚趾的骨或指甲。

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。

Frifting fingerweb flap is an ideal solutions to treat congenital incomplete cutaneous syndactyly.

指蹼皮瓣滑移术是治疗先天性不完全性皮肤性并指畸形的理想方法之一。

The typical clinical manifestations of SPD are soft tissue syndactyly between the third and fourth fingers,and between the fourth and fifth toes,with a supernumerary digit in the syndactylous web.p.Q317R point mutation located in the homeodomain of HOXD13 can result in typeⅤsyndactyly(MIM 186300),which is characterized by fusion of the fourth and fifth metacarpal.

本研究对HOXD13同源盒p.Q317R点突变和多聚丙氨酸延展突变进行功能研究，探索这两种突变导致不同并指畸形的分子机制。

In cases of mitten hand deformity as seen in Apert syndrome, the fingers and toes cannot be seen individually, which makes the prenatal diagnosis easier Fig.

在Apert综合征见到的并指畸形病例，手或趾不能被单个地观察到，它使得产前诊断更容易（图13）。48

Result: In the 3 categories and 10 exemples of congenital malformation fetus, The morphologic observation and histological observation of thymus in syndactylia, ectrodactylia and Siamese fetus was no obvious abnormity, but the morphologic observation and his-tological observation of thymus in anencephaly fetus appeared Obvious abnormity.

结果：三类、10例先天畸形胎儿中，并、缺指畸形和联体畸形胎儿胸腺的大体形态和组织学观察无明显异常，无脑畸形胎儿胸腺的大体形态和组织学观察出现明显异常。

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。

The skin lesions progressed with numerous grouped bullae, and erosions on a noninflamed base on the palms and soles which resulted in syndactyl deformities and flexion contracture of hands and feet.

皮肤的损害进展成许多的大水疱与手掌、足掌未发炎的糜腐蚀，导致手脚的并指畸形与屈曲挛缩。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。