查询词典 syndrome

Abnormal chromosome was detected in 17 fetuses. Among them, trisome 21, trisome 18, trisome 13, Turner syndrome, Klinefelter syndrome, short arm deletion of chromosome 18, and inverted chromosome 9 were detected in 8, 3, 1, 1, 1, and 2 fetuses, respectively. Abnormal chromosome was found in 5 out of 8 fetuses who received serum screening. Ultrasound showed abnormal chromosome in 11 fetuses.

共诊断17例胎儿染色体异常，其中21三体8例，18三体3例，13三体1例， 1 Turner综合征1例，Klinefelter综合征1例， 18染色体短臂微缺失1例，9号染色体臂间倒位2例(1例来源于母亲)。17例中有8例进行了唐氏儿血清学筛查，5例异常，11例超声检查胎儿有结构异常。

Other uncommon conditions including - achalasia (widening of the bottom of the oesophagus); tylosis; and Paterson-Brown Kelly syndrome (rare syndrome featuring iron deficiency and changes in the mouth or oesophagus).

其他罕见的条件，包括-贲门失弛缓症； t ylosis（ 1继承皮肤条件）；及百德-布朗凯利综合征（罕见的综合征特色缺铁和变化，在口腔或食道）。

HTP and yohimbine could significantly suppress acute and chronic tramadol withdrawal syndrome, while p-CPA could aggravate the precipitated withdrawal syndrome.

25-HTP与育亨宾能够明显抑制急性与慢性曲马朵依赖小鼠的催促戒断症状，p-CPA可以加重急性曲马朵依赖小鼠的催促戒断症状。

CFC syndrome and CS can be distinguished from NS by the presence of ectodermal abnormalities, mental retardation and a lack of familial cases. CFC syndrome can be distinguished from CS by the rare presence of papillomata, fetal pads, acanthosis nigricans, wrinkled palms and soles, and loose skin of the hands and feet.

心脏－脸－皮肤徵候群及科斯特洛徵候群二者均具有外胚层的异常，智障，及缺乏家族案例，这些可以和努男徵候群区别；而心脏－脸－皮肤徵候群患者罕见乳突瘤，胎儿垫，黑棘皮病，手掌脚掌皱纹及手脚疏松的皮肤，这些可以和科斯特洛徵候群区别。

Purpose: To observe the clinical therapeutic effect on primary nephrotic syndrome with adrenocortical hormone and the syndrome differentiation method.

目的：观察辨证论治合肾上腺皮质激素治疗原发性肾病综合征的临床疗效。

Complications following cerebral intravascular stent implantation included carotid sinus syndrome, hypertransfusion syndrome, cerebral angiospasm, thrombosis, and restenosis.

置入并发症主要有颈动脉窦反应，高灌注综合征，脑血管痉挛、血栓形成、再狭窄等。

Shortening of telomere may be one of pathomechanism of spleen Qi deficiency syndrome. The accumulation of free radical produced by the decrease of the antioxygen ability may be damage the telomere, and that may be one of the mechanisms of telomere shortening in liver of rat model with spleen Qi deficiency syndrome.

提示端粒长度缩短可能是脾气虚证的病理机制之一；脾气虚证状态下，机体的抗氧化能力下降、自由基蓄积损伤端粒可能是脾气虚证模型组大鼠肝组织端粒长度缩短的机制之一。

Results: The changes following hydrocortisone intervention of rats could be identified by PCA, and the kidney deficiency syndrome rats entered a state of "hyperfunction", involving a series of changes in metabolic pathway and metabolic network. The response integral area of lactic acid (δ 1.37) increased, indicating the accumulation of metabolites of lactic acid. The amount of dimethylamine (δ 2.72) also increased, indicating that the disorder of kidney function was related to kidney-deficiency syndrome. The response of creatinine (δ 3.87), asparaginic acid (δ 2.83), taurine (δ 3.44, 3.28), and hippurate (δ 7.84, 7.56, 7.64, 3.97) all decreased significantly, indicating that the hydrocortisone might cause adrenal cortex excretion injury. The response integral area of succinate (δ 2.41) and citric acid (δ 2.53, 2.68) decreased, which was usually caused by disorder of the mitochondrial function.

结果：PCA方法处理肾虚证和空白对照大鼠尿液数据显示，两组大鼠的数据可以在得分图实现分类，与对照组比较肾虚组大鼠由于氢化可的松诱导，大鼠机体进入一个过消耗后衰弱的状态，相关代谢发生显著变化，乳酸(δ 1.37)代谢发生堆积；二甲胺(δ 2.72)的含量增加，提示肾虚与肾功能异常是密切相关的；天冬氨酸(δ 2.83)，牛磺酸(δ 3.44， 3.25)，马尿酸(δ 7.84， 7.56， 7.64， 3.97)，肌氨酸(δ 3.87)等的相对积分面积明显下降，这预示糖皮质激素可能引起了肾上腺皮质分泌功能的损害；琥珀酸(δ 2.41)和柠檬酸(δ 2.53， 2.68)是三羧酸循环能量代谢及糖酵解的中间产物，其含量的降低，通常是由于线粒体功能紊乱所引起。

With Asperger Syndrome, the syndrome is the behavior.

而亚斯柏格症儿童的特征，就是他们的行为。

1、There is the close correlation of Diseases- syndrome among ShaoYin disease-yang asthenia syndrome and diabetic nephropathy.

四、结论 1、少阴病阳虚证与DN之间具有紧密的病证相关性 2、糖肾方颗粒可以显著改善DN患者的临床症状，提高患者的生活质量。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。