英语释义

1. absence of spermatozoa from the seminal fluid

2. absence of spermatozoa from the seminal fluid — compare aspermia

片语

azoospermia factor AZF无精子因子

non-obstructive azoospermia非梗阻性无精子癥

Obstrutive Azoospermia阻塞性无精癥

azoospermia fae-tor无精子因子

Seminal Vesiculitis blood Azoospermia精囊炎血精癥

idiopathic azoospermia原发无精癥

azoospermia factorAzoospermia factor (AZF) refers to one of several proteins or their genes, which are coded from the AZF region on the human male Y chromosome. Deletions in this region are associated with inability to produce sperm.

deleted in azoospermia基因

Obstructive Azoospermia阻塞性无精癥

英汉例句

• clinical material and methods: 38 male infertility patients with azoospermia were selected.

  临床资料和方法选择38例为无精癥。

• one of the important reasons of male infertility is azoospermia and dead spermatozoa.

  引起男性不育的一个重要原因是无精癥、死精癥。

• objective to detect the role of azoospermia factors located on proximal yq in spermatogenesis among chinese patients with idiopathic azoospermia and oligozoospermia.

  目的探讨国人特发性无精子癥和少精子癥患者y染色体长臂近端无精子因子基因变异情况。

• objective:to study the relationship between polymorphism of (cag)n repeats within androgen receptor gene with severe oligozoospermia or azoospermia patients.

  目的探讨无精或严重少弱精癥患者与雄激素受体基因（cag）n重复多态性的关系。

• objective: to observe the relationship between microdeletions of azf(azoospermia factor) on y chromosome in male with idiopathic azoospermia and severe oligozoospermia.

  目的：观察y染色体azf微缺失与原发性无精子癥和严重少精子癥之间的关系。

• methods both chromosome karyotypic and y-chromosome azf microdeletion analysis were performed on 91 blood specimens of idiopathic azoospermia and 42 patients of oligozoospermia patients.

  方法对91例无精子癥患者和42例严重少精子癥患者，采用外周血染色体核型分析和y染色体azf区域微缺失联合检测。

• objective to investigate the relationship between chromosome abnormalities and y chromosome microdeletion of azoospermia factor (azf) in patients with azoospermia and oligozoospermia.

  目的探讨无精、少精及严重少精癥与染色体核型异常和y染色体无精子因子（azf）微缺失的关系。

• methods daz gene region of y chromosome were detected by pcr technique in 45 azoospermia , 78 oligozoospermia patients and 20 normal fertile men.

  方法应用聚合酶链技术（pcr）对45例无精子癥、78例少精子癥、20例正常生育男性进行y染色体daz的微缺失检测。

• several factors have been proposed for male infertility and spermatogenic failure is confirmed to be a significant one, which typified by idiopathic non-obstructive azoospermia or oligozoospermia.

  引起男性不育的因素很多，其中一个重要的原因是精子生成障碍，主要表现为原发性非梗阻性无精子癥或少精子癥。

• in azoospermia and severe oligo-asthenospermic patients, chromosome abnormality showed numerical abnormalities and structural abnormalities which involved in most chromosomes.

  在无精子癥及严重少弱精子癥患者中，染色体异常表现有数目异常和涉及大多数染色体在内的结构异常。

• the analysis of correlation between karyotype and azf microdeletion on y chromosome for patients with azoospermia and severe oligozoospermia.

  目的：研究男性原发性无精及严重少精癥患者y染色体azf微缺失区域与临床表型的关系。

• methods azf microdeletion screening was carried out in 42 idiopathic azoospermia patients in chengdu area by using pcr and gelose gel electrophoresis.

  方法运用pcr及琼脂糖凝胶电泳等方法，对成都地区42例原发性无精子癥患者进行了azf基因微缺失筛查。

• in cases with incomplete gonadotrophin suppression, the chances of becoming azoospermia were 1.5 times higher in men with cag repeats number more than 22.

  在促性腺激素未被完全抑制组中，cag重复数大于22的受试者达到无精子癥的机会是其他受试者的1.5倍。

• objective: to find out the relationship between the male infertility and the ychromosome azoospermia factor(azf)microdeletion and its clinical application in east guangdong.

  目的：探讨粤东地区男性不育人群与y染色体无精子因子（azf）微缺失的关系和临床应用。

• objective to analysis the azoospermia of congenital bilateral absence of vas deferens, after epididymal sperm retrieval puncture across icsi to help pregnancy, and discuss its results.

  目的分析与诊断先天性输精管缺如性无精子癥，经附睪穿刺取精后行icsi助育，探讨其助育结果。

• methods cytogenetic analysis and multiplex polymerase chain reaction(pcr) analysis were done on the 148 patients with azoospermia and serious oligozoospermia.

  方法应用细胞遗传学和多重聚合酶链反应技术，对148例无精癥、严重少精癥患者进行检测。

• conclusion: fasl-844 polymorphism appears to be a genetic predisposing factor of idiopathic azoospermia or severe oligozoospermia among southern chinese han males.

  结论：fasl-844基因多态性可能是中国南方汉族男性特发性无精子癥及严重少精子癥的遗传易感因素之一。