性别异常

词组短语

sexual abnormality

与性别异常相关的网络例句 [注：此内容来源于网络，仅供参考]

The results were analyzed with the statistical software package spss10.0.results ①between two groups,there was no significant difference about the affection of age,sex and the destribution and location of aneurism on prognosis outcome(p＜0.05).however,the grading of hunt hess and fisher in group a(gos＞3) showed significantly lower than in group b(gos≤3),（p＜0.001）;② there was no significant difference in the frequency of heart rate, st elevation, st depression,t wave inversion,u wave inversion and ventricular arrhythmia(p＞0.05).the frequency of abnormal q wave, supraventricular arrhythmia and the ecg scores in group a showed significantly lower than in group b （p＜0.05,p＜0.001）;③the ecg scores was the most powerful multivariate risk stratified(ecg ≥5 vs ecg＜5; p=0.002,or=0.010,95%ci 0.001~0.173).conclusion the ecg score, a new and simple method of semi quantification, was a powerful risk predictor for patients with sah.

应用spss10.0 统计包分析结果。结果①在年龄、性别、动脉瘤生长部位影响动脉瘤性sah预后方面，两组病例无明显差异（p＞0.05）。而按sah后hunt hess分级和fisher分级，gos＞3病例的分级要明显低于gos≤3的病例的分级（p＜0.01）；②两组在心率、st段抬高、st段压低、t波倒置、u波倒置、室性心律失常出现的频率无明显差异（p＞0.05）；在异常q波和室上性心律失常出现频率及心电图评分方面，gos＞3的组别明显低于对照组（p＜0.05，p＜0.001）；③心电图评分是sah患者预后最显著影响的变量（p=0.002，or=0.010，95%的可信区间0.001~0.173）。结论心电图评分作为一种新型、简便的半定量方法，能有效的预测蛛网膜下腔出血病人的预后。关键词：心电图；预后；评分；蛛网膜下腔出血

Methods:To induce 17 515 adult physical exam materials that were collected by our Physica Examination Center from 2001 to April 2007 in LianYunGang cantonal,and analyze the detectable ratios of hypetension,hyperglymia and hyperlipemia and their relation with the detectable ratios of gender, age,occupation and heart abnormity.

归纳本中心2001～2007年4月本市区不同职业成人17 515例体检资料，分析高血压、高血脂、高血糖的检出率与性别、年龄、职业的关系和与左心室肥大和心肌缺血二项心电图异常检出率的关系。

Assignment of SRY as the testis-determining factor in eutherian mammals is supported by molecular analysis of cytogenetic sex reversal (i.e., XX males and XY females) and by complementary studies of transgenic murine models.

Sry转基因小鼠的产生和对包括XX男性及XY女性等多种性分化及发育异常患者的研究，都支持SRY基因是TDF基因及其在性别决定中的开关控制作用。

So,detection of SRY gene may play an important role in the study of hypospadias.

2先天性尿道下裂是一种性别发育异常，尿道缺失是性腺发育不全表现。

Disorders can be autosomal recessive or dominant, sex-linked, or maternally inherited.

这些异常可能是自体隐性或显性疾病、与性别有关、或母系遗传。

There is a cognitive disorder in 85.7 percent of microcephaly children with atelencephalia that is influenced by multifarious factors.

结果 42例患儿发育商值异常者占85.7%（36/42），影响早期认知功能的因素主要包括患儿有异常头颅影像学改变、性别、初诊年龄。

Compared with the 44 patients on sirolimus therapy with no evidence of a disorder, the 4 patients (8.3%) who developed suspected sirolimus-associated interstitial pneumonitis showed no difference in gender, immunosuppressive therapy, days posttransplantation, comorbidity, or preexistent lung disease.

相比于其他44名西罗莫司治疗而无异常病症的患者，该4名发展为西罗莫司相关间质性肺炎患者（8.3％）在性别、免疫抑制治疗、移植后天数、原发病以及肺原发疾病上无明显差异。

The absence or mutation of SRY gene may be concerned with the pathogenesis of hypospadias which is a sex upgrowth abnormality.

(1)SRY基因不是性别决定的唯一基因，SRY基因缺失或突变可能导致性发育的一系列异常改变，尿道下裂的发生与SRY的缺失、变异有关。

Results Patients who had at least one abnormal result of liver function test accounted for 70.99% in untreated group and 61.07% in treated group. The most common abnormal hepatic function parameter in patients with thyrotoxic hepatic lesion was increased alkaline phosphate enzyme, which was 57.3% in untreated group and 51.0% in treated group. Abnormalities of alanine transaminase, aspartate transaminase, gamma-glutamyl tyanspeptidase and total bilirubin were 28.2%(37/131), 18.3%(24/131), 10.7%(14/131) and 21.4%(28/131) in untreated group and 21.5%(32/149), 15.4%(23/148), 4.7%(7/149) and 20.1%(30/149) in treated group, respectively. The possibility of thyrotoxic hepatic dysfunction was correlated with the patients' age and FT3 and FT4 levels, but not with the genesis and course of disease, sex, family history of hyperthyroidism, or levels of TGAb and TMAb. Conclusion Abnormal results of liver function test are commom in patients with hyperthyroidism.

结果 在未治组甲亢性肝功能损害的发生率为70.99%，经治组为61.07%；甲亢性肝功能损害最常见的异常指标是碱性磷酸酶增高，未治组、经治组分别为57.3%、51.0%；血清谷丙转氨酶异常在两组的发生率分别为28.2%、21.5%；血清谷草转氨酶异常在两组的发生率分别为18.3%、15.4%；总胆红素异常在两组的发生率分别为21.4%、20.1%；谷酰胺转肽酶异常的发生率未治组和经治组分别为10.7%、4.7%；甲亢性肝功能损害的发生与病程、甲状腺疾病家族史、性别、TGAb水平、TMAb水平无关，与年龄、甲状腺激素水平有关。

The effect of treatment is negatively correlated with the course of disease, generally, the effect is much worse with the course of disease is much longer; The effect is positively correlated with the course of treatment, it is better if the course of treatment is longer.The group of more than one year is much excellent than the group of less one year. The ex-electroencephalogram before treatment is normal, on edge and a little abnormal, the effect is better. As regards CT or MR result, there is difference between the effective group and the ineffective group. The result of CT and MR is negative, the effect is better, and the effect to demyelination and leukoencephalopathy is most worst.However,for the tipe of much abnormality, the effect is the most worst.The effect is related to course of disease.The effect is better if the course is shorter.There is no difference in the tipe of disease the symptoms before episode, the frequency of episode, the inducing reasons, the age, sex and so on.

病程的长短与疗效存在负相关关系，病程越长疗效越差；疗程与疗效存在正相关关系，疗程越长疗效越好；疗前脑电图的异常程度与疗效存在负相关关系，正常、边缘及轻度异常者，疗效较好，重度异常者疗效最差；无效组与有效组在CT及MR检查结果上有差异，有阴性者疗效好，阳性者疗效差，脱髓鞘及脑白质病疗效最差的趋势；疗效与性别无相关性；无效组与有效组在发作类型、既往病史、辨证分型、发作先兆、疗前发作频率、诱因、发病年龄、就诊前所用药物方面无差异。

与性别异常相关的网络解释 [注：此内容来源于网络，仅供参考]

addiction：成瘾性

机体方面的因素有:性别年龄、遗传异常、病理情况、心理因素(安慰剂、placebo)以及机体对药物反应的变化:致敏反应(sensitization),快速耐受性(tachyphylaxis)、耐受性(tolerance)、习惯性(habituation)、成瘾性(addiction)、依赖性(dependence).

biosynthesis：生物合成

表型上,这些男性是毫无疑问地最常见,且有潜力变得最严重的性别分化异常被证实是在具有皮质醇(cortisol)生物合成(biosynthesis)酵素缺陷的 46,XX 个体(38, I 17).

deletion：缺失突变

具有 WT-1 缺失突变(deletion)的小鼠不会形成产生性腺的中胚层,因此表示它可能是SRY 的上游而非下游基因. 具有 46,XY 核型,以及体染色体遗传短指发育不良(campomelic dysplasia)合并性别倒错的个体同时会产生大范围的骨骼异常.

habituation：习惯性

机体方面的因素有:性别年龄、遗传异常、病理情况、心理因素(安慰剂、placebo)以及机体对药物反应的变化:致敏反应(sensitization),快速耐受性(tachyphylaxis)、耐受性(tolerance)、习惯性(habituation)、成瘾性(addiction)、依赖性(dependence).

seminiferous tubule：细精管

性腺组织必须表现出卵巢滤泡与细精管(seminiferous tubule). 透纳氏症(Turner's syndrome)的病人表现出性别分化异常,乃是因为一性染色体缺失症候群,其结果导致异常性腺发育(见表 16.1). 在这些病患,卵巢刚开始发育时拥有正常的卵母细胞(oocyte)存量(14).

tachyphylaxis：快速耐受性

机体方面的因素有:性别年龄、遗传异常、病理情况、心理因素(安慰剂、placebo)以及机体对药物反应的变化:致敏反应(sensitization),快速耐受性(tachyphylaxis)、耐受性(tolerance)、习惯性(habituation)、成瘾性(addiction)、依赖性(dependence).