- 更多网络例句与多指畸形相关的网络例句 [注：此内容来源于网络，仅供参考]
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Profound mental retardation, scalp defects, holoprosencephaly, sloping forehead, anophthalmia/microphthalmia, absent nose, cyclopia, proboscis, bulbous nose, cleft lip/palate, cardiac abnormalities, omphalocele, ambiguous genitalia, postaxial polydactyly, neural tube defects
极重度精神发育迟滞；头皮缺失；前脑无裂畸形；前额倾斜；无眼/小眼；无鼻；独眼畸形；长嘴；球状鼻；唇腭裂；心脏异常；脐疝；两性生殖器；轴后多指畸形；神经管缺陷
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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
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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。
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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。
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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。
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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。
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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。
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Birthmark, indirect inguinal hernia,harelip,external ear deformity and hyperdactylia or syndactylia were the most commonly seen types of deformities.
畸形中以胎记、腹股沟斜疝、唇裂、外耳畸形及多指为多见，主要分布于0～ 19岁人群。
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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。
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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。
- 更多网络解释与多指畸形相关的网络解释 [注：此内容来源于网络，仅供参考]
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polydactylism：多指畸形/多趾畸形/赘生指
polydactylia 多指畸形 多趾畸形 | polydactylism 多指畸形 多趾畸形 赘生指 | polydactyly 多指趾畸形
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Polydactylism; Hyperdactylism：多指(趾)(畸形)
Polycory 多瞳(畸形) | Polydactylism; Hyperdactylism 多指(趾)(畸形) | Polyembryony 一卵多胎
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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,
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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.
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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.
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polydactyly：多指畸形/多趾畸形
物理图谱 physical map | 多指畸形/多趾畸形 polydactyly | 性染色体 sex chromosome
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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.
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Polyphalangism; Hyperphalangism：多指(趾)骨(畸形)
Polypathy 多发性病; 复杂病 | Polyphalangism; Hyperphalangism 多指(趾)骨(畸形) | Polyphasic anaplasy 多形退行发育
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polyphalangism：多指[趾]骨畸形
doggie <儿语> 小狗, 狗, 汪汪 | polyphalangism 多指[趾]骨畸形 | EAHC East African Harbours Coporation 东非港口公司
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Polythelism; Superfluous nipple：多乳头(畸形)
Polysyndactyly 多数并指(趾)(畸形) | Polythelism; Superfluous nipple 多乳头(畸形) | Polytrophy; Excessive nutrition 养料过多