查询词典 family history

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。

Diagnosis/testing. A diagnosis of ocular albinism is probable in the presence of congenital nystagmus, iris translucency, and significant hypopigmentation of the ocular fundus periphery in males with normal skin pigmentation and foveal hypoplasia, reduced visual acuity, and aberrant optic pathway projection, as demonstrated by crossed asymmetry of the cortical responses on visual evoked potential. X-linked inheritance is documented by either a family history consistent with X-linked inheritance or the presence of typical carrier signs (irregular retinal pigmentation and partial iris transillumination) in an obligate carrier female.

诊断/检测。对于皮肤色素沉着正常、中央凹发育不全、视敏度降低以及视径投射异常（VEP，表现为视觉诱发电位中皮层反应的交叉不对称）的男性患者，当存在先天眼球震颤、虹膜半透明以及显著的眼基底层边缘色素减退的症状时，可被疑似诊断为眼白化病。X连锁性遗传则以存在与X连锁遗传一致的家族病史，或在一个应当为携带者的女性中存在典型的携带者迹象（视网膜色素沉着不规则以及部分虹膜透射）而被确认。

The incidence of abnormal lipid trigone in children with a family history of premature CHD or non premature CHD and the controls were 52.6%, 10.9% and 1.2%, respectively.

有早发CHD家族史者LDL-C/HDL-C(2.85±1.21)高于无早发家族史组(1.37±1.11)和对照组(0.96±0.68)(P均。01)，HDL-C水平［(1.11±0.26) mmol/L］低于无早发家族史者［(1.59±0.47) mmol/L］和对照组［(1.72±0.53) mmol/L］。

You may be more at risk of testicular cancer if you have an undescended testicle, a family history of the disease or a previous testicular tumour.

你可能会更危险的睾丸癌如果您有一个未降睾丸，一个家庭的历史，疾病或先前睾丸肿瘤。

Result Unhealth emotinal state,hepatic disease and family history of PHC were the strong independent factors,and they also had obvious interaction.

结果不良精神因素、肝脏疾病史和肝癌家族史与肝癌发生均有明显作用，而且三个暴露因素既是作用很强的独立因素，亦是明显的相乘作用。

The professor would not rule out that smoking dope may prevent Alzheimer's disease if the disease is in a person's family history.

这位教授不排除吸烟涂料可以防止老年痴呆症的疾病，如果是在一个人的家族病史。

I have a family history of blood clots. Should I take the pill?

我有家族血栓史，我能服用避孕药吗？

You should tell your GP if you have any family history of blood clots including DVT.

你应该告诉你的家庭医生如果您有任何家族病史，血液凝块，包括深层静脉血栓现象。

When she was one year old,there was obvious inflammatory at the edge of cutinized layer ,which begun to expand to dorsal aspects of hands and feet.She had no family history.

十二个月大学步，炎症明显，角化层目前有向手、脚背扩展趋势，用过多种外敷药，效果不明显，我们夫妇及上两代都无此症状。

The story of how the Vautiers began generations ago to make a living pulling cod from the waters off Newfoundland, hefting each sleek green-and-white fish by hand as it came off the line, is lost in family history.

如何vautiers故事开始前几代拉谋生鳕从海面纽芬兰楼上每个漂亮的绿色和白色的手像鱼出刊的路线、失去家庭的历史。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。