多指畸形的

基本解释 (translations)

polydactyl  ·  polydactylous

与多指畸形的相关的网络例句 [注：此内容来源于网络，仅供参考]

Limb abnormalities including phocomelia, amelia, clubfeet, polydactyly, microtia, facial palsy, orofacial cleft, microphthalmia, cardiac defect, IUGR, urogenital, gastrointestinal, and spinal defects

四肢异常包括：短肢畸形；无肢畸形；畸形足；多指畸形、小耳畸形；面部麻痹；口面裂；小眼畸形；心脏异常；宫内生长受限；泌尿生殖系的、胃肠道的和记脊柱的缺陷

Objective To discuss the classification and treatment for congenital polydactyly.

目的 介绍先天性多指畸形的分类，讨论其治疗方法。

Objective To investigate the epidemiologyical characteristics of polydactyly.

多指是一类常见的先天畸形，影响患者手足外观和指趾功能。

CHF-associated diseases were Caroli's syndrome, polycystic kidney disease, caernous transformation of the portal ein, Joubert's syndrome, on Meyenburg complex, polydactyly, medullary sponge kidney, and pancreatic duct atrophy.

先天性肝纤维化相关的疾病包括Caroli's综合症、多囊肾、海绵状门静脉形成、Joubert's综合症，on Meyenburg 复合物，多指趾畸形，髓状海绵样肾，胰管萎缩。2例发展成胆管癌。

Congenital syndactyly is a common hand deformity,has variety and large degree of variation,and often associated with a variety of other malformations,may seriously affect the hand function.

先天性并指是手部畸形中最常见的类型之一，种类多，变异度大，且常常合并其他多种畸形，严重影响手功能的发挥。

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。

How common means of fetal deformities, equinus, pyloric stenosis, boys urethra

常见的胎儿畸形有多指、马蹄足、幽门狭窄、男孩尿道

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。

与多指畸形的相关的网络解释 [注：此内容来源于网络，仅供参考]

blending inheritance：融合遗传

"换句话说,詹金主张普遍出现后来遗传学文献称之为"融合遗传"(blending inheritance)的现象. 考虑到詹金选用六个手指的个体作为典型的畸变例证,则这种说法尤其令人感到惊讶,因为自莫培兑和Reaumur以来早已知道多趾畸形(六指也属于此)是没有中间型的遗传.

cerebral haemorrhage：脑溢血

看情况定,脑出血又称脑溢血(cerebral haemorrhage)是指非外伤性脑实质内出血,死亡率高. 绝大多数由高血压合并动脉硬化引起,仅有少数为其他原因的先天性脑血管畸形等所致. 本病以 50岁以上的高血压病人最多见,多在情绪紧张、兴奋、排便、用力时发生.

osteogenesis imperfecta：骨发育不全

例如骨发育不全(osteogenesis imperfecta)、克汀病(cretinism)、巨结肠(hirschsprumg disease)等. 发育过度性畸形:由器官或器官的一部分增生过度所致,例如在房间隔形成期间第二隔生长过度而引起的卵圆孔闭合或狭窄、多指(趾)畸形等.

polydactyly：多指

II型:远节指骨完全重复,各有其独立的骨骺,分别与近多指(Polydactyly)为最常见的手部先天性畸形,多发生在手部的桡侧,有时合并其他畸形. 临床上可分为三种类型:①多余手指仅有软组织,没有骨骼. ②多余指中有部分指骨、部分肌腱,

polydactyly：多指趾畸形

而王瑞生医师则说,胎儿手部畸形的发生率并不高,仅约0.7%左右,常见的状况有曲指畸形(camptodactyly)、并指畸形(syndactyly)以及多指(趾)畸形(polydactyly)等.

polydactyly：多指[畸形]

多指畸形(polydactyly)在手的先天性畸形中最为常见,有时可与并指、短指或其它先天性畸形同时存在. 提供表达稳定的家族性多指畸形谱系可以为进一步研究相关基因的定位和功能提供研究基础. 现将双手三节拇指多指畸形一家系16例报道如下.

syndactyly：并指[畸形]

治疗说明本症需作成形手术. 手术时间须视畸形程度而定. 指尖并指对手指发育妨碍较大,应及早手术. 一并指畸形(Syndactyly)是多见的畸形,在2000个新生儿中可有一例. 本症与遗传有关,往往是双侧性的.

mesenteric cyst：肠系膜囊肿

肠系膜囊肿(mesenteric cyst)是指位于肠系膜、具有上皮衬里的囊肿. 绝大多数为良性病变,多因先天性畸形或异位的淋巴管组织发展而成,也有因腹部外伤、淋巴管炎性梗阻或局限性淋巴结退化而形成. 肠系膜囊肿较少见,为一种良性疾病,70%见于成人,

microcephalus：脑小畸形

脑小畸形(microcephalus)一种是先天性脑发育不良,为真性脑小畸形,另一种为脑发育停止. 脑小畸形系指脑重量小于正常,多同时伴有头围小. 正常情况下,无退变损害的成人脑重量一般不低于900g,低于此限为脑小畸形. 有时脑小畸形者脑重量仅有300~400g或更少.

microstomia：小口畸形

小口畸形(microstomia)是指口裂过小先天性小口畸形是山胎儿发育障碍所致较少见后天性小口畸形多由口角瘢痕挛缩所致表现为口角处蹼状瘢痕上下唇在门角处粘连.严重者伴有唇组织的缺失小口畸形不仅影响美观而且影响言语及进食需要手术