先天性输精管缺如,congenital absence of the vas deferens
1)congenital absence of the vas deferens先天性输精管缺如
1.Objective: To investigate the clinical characteristics,diagnosis and therapeutic strategies ofcongenital absence of the vas deferens(CAVD).目的:探讨先天性输精管缺如(CAVD)的临床特点,提高其诊断和治疗水平。
英文短句/例句
1.Screening Mutation of CFTR Gene in Man with Congennital Bilateral Absence of Vas Deferens;先天性输精管缺如患者CFTR基因突变筛查
2.Determination of semen biochemical indicators in infertile males with congenital bilateral absence of vas deferens先天性双侧输精管缺如患者精浆生化指标测定
3.Diagnosis and Treatment of Primary Obstructive Megaureter;先天性梗阻性巨输尿管的诊断与治疗
4.Radiographic Analysis of Congenital Deformity of Kidney and Ureter肾脏及输尿管先天性畸形的X线分析
5.Diagnosis of Congenital Anomaly of Lower Ureter with MRI and MSCT输尿管下端先天性异常的MRI和MSCT诊断
6.The absence or closure of a normal body orifice or tubular passage such as the anus, intestine, or external ear canal.（先天性）闭锁，无孔正常的身体孔或管道，如肛门、肠或外耳道的缺失或闭合
7.High-frequency ultrasonography diagnosing congenital deformity of ureter in infants高频超声显像诊断婴幼儿先天性输尿管畸形
8.congenital absence of endometrium先天性子宫内膜缺失
9.inborn error of amino acid metabolism先天性氨基酸代谢缺陷
10.congenital absence of organ of Corti先天性柯替氏器缺失
11.congenital agammaglobulinemia先天性血γ－球蛋白缺乏
12.congenital aprothrombinemia先天性凝血酶原缺乏症
13.congenital defects, blindness, etc先天性缺陷、 失明等.
14.congenital hydrocele of spermatic cord先天性精索鞘膜水囊肿
15.Investigation of Neural Factors in Pathogenesis of the Congenital Ureteropelvic Junction Obstruction先天性肾盂输尿管连接处梗阻性肾积水的神经性因素探讨
16.The Misdiagnosis of Congenital Absence of Gallbladder by Clinic and Ultrasound Exam (Reports of 4 cases)先天性胆囊缺如临床和超声检查误诊分析(附4例报告)
17.reversibility of vasectomy可逆性输精管绝育术
18.Evaluation of the Effectiveness and Safety of Catheter Closure in 32 Cases of Secundum Atrial Septal Defect经导管封堵治疗先天性继发孔型房间隔缺损32例的疗效观察
相关短句/例句
congenital bilateral absence of the vas deferens先天性双侧输精管缺如
1.Study on epididymal sperm function of infertile males withcongenital bilateral absence of the vas deferens;先天性双侧输精管缺如不育患者附睾精子功能及妊娠率的研究
3)congenital unilateral absence of the vas deferens先天性单侧输精管缺如
1.Objective To analyze the frequency and hot spots of cystic fibrosis transmembrane conductance regulator(CFTR) gene in Chinesecongenital unilateral absence of the vas deferens (CUAVD) patients.目的探讨囊性纤维跨膜转运调节物 (cystic fibrosis transmembrane conductance regulator,CFTR)基因在中国人先天性单侧输精管缺如 (congenital unilateral absence of the vas deferens,CUAVD)患者中的突变频率及热点。
4)Congenital bilateral absence of the vas deferens (CBAVD)先天性双侧输精管缺如(CBAVD)
5)Vas deferens absence输精管缺如
6)Congenital absence of gallbladder先天性胆囊缺如
延伸阅读
先天性单肾缺如先天性单肾缺如congenital unilateral renal agenesis临床多无症状，因之其发病率在各作者报道中差异较大，为(1∶450）～(1∶1800）。虽然单肾更多见于男性，但女性由于合并生殖器畸形如子宫发育不良及阴道不发育等而进行检查者机会较多，因而易被发现。单侧肾不发育的严重性在于当孤立肾有病变或受到外伤后，因不了解病儿只有一个肾而轻易施行肾切除。这种严重错误在临床工作中是发生过的。因此，进行肾切除手术前必须查明对侧肾脏的情况。
