查询词典 syndactyly

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。

To determine the early changes and process of formation of central polydactyly, syndactyly, and cleft hand, we experimentally induced these anomalies in the hind limbs of rat embryos and discussed the relationship among these abnormalities.

目的：在同一个病人有多种中心型多趾、并趾、裂手畸形组合常出现在各自的四肢，然而很少知道在四肢发育的过程中的趾线的异常诱导的早期变化，为了确定中心型多趾、并趾以及裂手畸形的形成过程和早期变化，我们通过实验在大鼠的下肢诱导这些异常并探讨这些异常之间的关系。

The complex type of syndactyly may be associated with other finger or toe abnormalities including polydactyly, oligodactyly, or duplicated phalanges as well as abnormally shaped bones.

复合型并指畸形可能与合并其它手指或脚趾异常，包括多指、少指、重复指和异形骨。

IUGR, tetraphocomelia, or hypomelia caused by mesomelic shortening of the limbs with radial defects and oligodactyly or syndactyly (the upper limbs are more severely affected than lower limbs), cleft lip/palate, large genitalia, congenital heart defects, cystic kidneys, characteristic face with hypertelorism, a prominent premaxilla, a mid-face capillary hemangioma, cloudy corneas or cataracts and dysplastic or small ears, micrognathia, beaked nose, ear malformations, and mental retardation

宫内生长受限，由于四肢中间缩短引起的四肢短小畸形或短肢畸形并桡骨缺陷和少指畸形或并指畸形（对上肢的影响比下肢更严重），唇腭裂，生殖器肥大，先天性心脏病，囊状肾，特征面容：眶距过宽、前额突出、脸中部毛细血管瘤，角膜混浊或白内障和小放的或发育不良的耳，小颌畸形，钩状鼻，耳畸形和精神障碍。

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。

Objective To discuss the classification and treatment of congenital syndactyly.

目的 探讨先天性并指畸形的分类与治疗方法。方法 1988年 1月至 1999年 3月共手术治疗先天性并指畸形 2 4例。

Prenatal diagnosis of simple toe syndactyly is almost impossible, whereas prenatal diagnosis of finger simple syndactyly is possible but very challenging.

产前诊断简单型并趾畸形几乎不可能，然而产前诊断单纯型并指畸形是可能的额，但是具有挑战性。

Methods From January 1988 to March 1999, 24 cases of congenital syndactyly were treated and classified by fusion tissue combined with the degree of fusion as follows:①simple complete syndactyly (4 cases).

结合并连的组织和程度分为：(1)单纯性完全性并指 4例，2指并指一次手术，3指并指分二次手术。(2 )单纯性不完全并指 9例，一次手术。(3 )复杂性完全并指 4例，分期手术。(4 )复杂性不完全并指 0例。(5 )复合性并指 7例，单纯行并指分指术。

The most severe form of syndactyly is classified as complicated syndactyly which refers to fingers joined by bony fusion other than a side-to-side and can include bony abnormalities such as extra, missing, or duplicated phalanges and abnormally shaped bones such as delta phalanges.

最严重的并指类型被归为复杂并指畸形，它表示手指除了由骨并排连接外，还可包括骨的异常，例如：多出一部分、缺失或重复指，以及异常形状的骨，如三角骨。

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。

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。