查询词典 congenital syphilis

Etiological classification revealed that 4 cases were congenital(2.12%), 22 cases...

病因分类，先天性 4例占 2 。12 %，继发性 2 2例占11.34 %，特发性 16 8例占 86 。6 0 %。

Mother with this disease whose baby may infect diffuse pyoderma , with symptom of excoriation , so it often be considered as congenital syphilisby mistake .

孕妇感染后可引起胎膜早破而导致早产，患病母亲所生小儿可患有弥漫的脓皮病，表皮脱落，常被误认为是先天梅毒。

Congenital fibrosis syndrome is a rare familial hereditary disease, characterized by fibrotic change of extraocular muscles.

摘要先天性纤维化症候群是一少见的家族性遗传疾病。

Fibromuscular dysplasia is a congenital disorder involving thickening of the arterial wall and is a cause of renal artery stenosis in younger adults, particularly women 20 to 40 years old.

纤维肌性发育不良是一种涉及动脉壁增厚的先天性疾病，是引起年纪较轻的成人发生肾动脉狭窄的原因之一，特别是在20－40岁的妇女中。

Using the following methods to treat one patient of congenital absence of the tibia with fork-shaped lower femur, the caput fibulae forming unstable knee joint, and concomitant knee flexion 95 degree.

方法1例先天性右胫骨完全缺如，股骨下端呈叉状，腓骨头与股骨下端形成不稳定的膝关节，伴屈膝畸形95 ，于1岁半实施股骨下端修整术，5岁和8岁时分两期安装Ilizarov膝关节牵伸器，牵拉矫正屈膝畸形达到伸膝0 位，使腓骨头与股骨下端成膝关节，拆牵伸器后装配能稳定膝关节的下肢补高矫形器行走。

Of the binocular diplopia, there were 17 cases of strabismic diplopia and 2 cases of diplopia due to central fusional impairment. Of the cases with monocular diplopia, there were 4 cases resulted from operative complication and one case with congenital iridocoloboma.

结果 双眼复视19例中，斜视性复视17例，中枢融合障碍性复视2例；斜视性复视中，除3例为间歇性外斜视外，其余14例均有不同程度的眼肌运动障碍；单眼复视5例中，4例为手术后人工晶体偏位所致，1例为先天性下方虹膜缺损所致。

Methods: Combined with the morphological character of the gangliocyte in the intestinal wall under microscope, the stained result and distributed character of the diseased intestinal segment in clinical and pathological diagnosed as congenital macrocolon was stained and compared with S-100 and NSF and with the immunohistochemistrical technique.

结合光镜下肠壁神经节细胞的形态特征，并应用免疫组化技术对25例临床及病理诊断为先天性巨结肠的病变肠段行S-100和NSE染色，比较染色结果和分布特点。

congenital omphalocele, gastroschisis is a critical emergency, the appropriate surgery, ventilator support, the TPN therapy.a higher cure rate.

先天性脐膨出、腹裂虽然是危重的急症，经合适的手术、呼吸机的支持、TPN的治疗，有较高的治愈率。

In our study, 3 genotypies have been respectively demonstrated in UL139 and UL149 for the first time, and the corelations between certain genotypical structure and certain diseases were also proposed; The existence of the 3 genotypes of UL144 was foremost verified in isolates from congenital infants; Furthermore, the UL140, UL141 and UL145 genes were observed to be greatly discrepant to those had been described previously: comparing with Toledo, 231 nt are inserted in UL140, 2 more ORFs are obtained in UL141, and the UL145 ORF moves upstream by 90 nt. Except UL144, the sequences of 18 else genes in clinical isolates were submitted for the first time, and 479 sequences were assigned by GeneBank in total. Relevantly, 9 papers were published.

我们在学术界首次证实了HCMV UL139、UL149两个基因在临床分离株中分别存在三种基因型，发现了其中某个基因型的基因结构与特定来源的分离株存在一定的对应关系；首次在先天感染分离株中验证了UL144三种基因型的存在；首次证实了UL140、UL141和UL145等基因与原先认识的基因结构不同，其中UL140基因较Toledo株增加了231个碱基、UL141产生2个新的基因编码区、UL145 ORF较Toledo株前移90个碱基；首次或最先提交了除UL144基因外其余18个基因的临床分离株序列，本项目组共有479个HCMV相关基因序列被GenBank收录；发表研究论文9篇。

Congenital dyserythropoietic anemias are phenotypically and genotypically heterogeneous diseases.

先天性红细胞生成不良性贫血是显型和基因异构性疾病。

Although translator has turned from being a crystal ball by which the original culture can unrestrainedly penetrate to another crystal ball by which the target culture can freely traverse, the translator's personal embodiment, in the process of cognitive act, are still absent in translation studies. Translators are still subjects without body or simply disembodied subjects.

译者虽然由原语文化可以自由穿透的玻璃球变成了译语文化可以自由穿越的玻璃球，但译者认知过程中的个体体验在翻译研究中依然缺席，译者依然仅仅是一个没有躯体体验的主体。

Chillingly, he claimed our technology is 'not nearly as sophisticated' as theirs and "had they been hostile", he warned 'we would be been gone by now'.

令人毛骨悚然的，他声称我们的技术是'并不那么复杂，像他们一样，和"如果他们敌意"，他警告说，'我们将现在已经过去了。