遗传性

Benign hereditary chorea is an autosomal dominant disorder of early onset characterised by non progressive choreic movements with normal cognitive function occasionally associated with hypothyroidism and respiratory problems.

良性遗传性舞蹈症是一种早发的常染色体显性遗传性疾病，以非进展性的舞蹈样运动为特点，偶尔伴有甲状腺机能减退和呼吸系统疾病，但认知功能正常。

Methods Study subjects are all Chinese including 16 infants with sporadic congenital deaf-mutism, 39 patients with autosomal recessive hereditary hearing loss, 30 patients with autosomal dominant hereditary hearing loss and 100 normal adults.

收集中国散发先天性聋哑儿童16例，常染色体隐性遗传性聋39例(39个家系)，10岁前开始听力下降的常染色体显性遗传性聋30例(30个家系)和健康对照组100例。

Epidermolysis bullosa represents a group of genodermatoses characterized by fragility, easy blistering of the skin and mucous membranes.

遗传性大疱型表皮松解症是一组皮肤、粘膜脆性增加，容易出现水疱大疱的遗传性皮肤病。

Hereditary Hemochromatosis is the most common genetic disorder of persons of northern European extraction.

遗传性血色病是最常见的遗传性疾病的人的北欧提取。

The present invention selects and uses hereditary hypertension rat and rat with normal blood pressure to make hybridization, and the rat whose blood pressure is normal and arterial pressure susceptivity reflection sensitivity is less than 0.3 ms/mm Hg can be screened out from filial generation, bred and propagated, and repeatedly bred and propagated, after above 12 generations so as to obtain the invented pure rat with stable hereditary property and spontaneous arterial pressure susceptivity reflection functional defect.

本发明涉及医学实验动物模型技术领域，是培育用于心血管疾病防治研究的一种自发性动脉压力感受性反射功能缺陷的纯种大鼠的方法。本发明选用遗传性高血压大鼠和正常血压大鼠杂交，从子代中筛选出血压正常、动脉压力感受性反射敏感性低于0.3ms/mmHg的大鼠培育繁殖，并反复按此标准在其下一代中筛选、繁殖，经12代以上便得到遗传性稳定的自发性动脉压力感受性反射功能缺陷纯种大鼠。

Hypertension is a polygene transmissibility illness with complexity trait.

高血压病是一种遗传性疾病，属于复杂性状疾病范畴，是"基因-基因"与"基因一环境"相互作用所致的多基因遗传性疾病。

Gene diagnosis and functional study were conducted in different pedigrees of inherited hemorrhagic and thrombotic diseases including 21 of rare coagulation factor deficiencies, 2 of Glanzmann thrombasthenia, 2 of hereditary hemorrhagic telangiectasis, 13 of AT deficiency, 16 of PC deficiency, 3 of PS deficiency and 2 of combined PC/PS deficiency.

遗传性出血病方面，对21个少见的遗传性凝血因子缺陷症家系、2个血小板无力症家系、2个出血性毛细血管扩张症家系进行了相关基因与功能的研究。遗传性血栓病方面，对13个AT缺陷家系、16个PC缺陷家系、3个PS缺陷家系和2个PC/PS联合缺陷家系进行了相关基因诊断与功能的研究。

Study on clinical character and genetic model of Dyschromatosis Symmetrical Hereditaria and Freckle Pigmentary inherited disease, which occupies a part of population in genodermatosis, is disease of monogenic inheritance. The genes of some diseases have been identified, such as Xeroderma, incontinentia pigmentation and PJS syndromes.

色素性遗传性疾病在遗传性皮肤病中占有不小的比重，这类疾病大都属单基因遗传病，而且有些疾病的遗传基因已经被找到，如着色性干皮病、色素失禁症、PJS综合症等。

To inquire into the hereditary type of one familial hereditary cataract pedigree and the development pattern of ablepsia.

探讨1例家族遗传性白内障系谱的遗传性类型及致盲规律。

All hereditary RB are bilateral, or multifocal, 15% of unilateral RB is hereditable and 85% of unilateral RB is non hereditable.

所有遗传性的RB的发病都是累及双眼或多病灶的，15%的单眼发病的RB是遗传性的和85%的单眼发病RB则不是遗传性的。

Breath, muscle contraction of the buttocks; arch body, as far as possible to hold his head, right leg straight towards the ceiling (peg-leg knee in order to avoid muscle tension).

呼气，收缩臀部肌肉；拱起身体，尽量抬起头来，右腿伸直朝向天花板（膝微屈，以避免肌肉紧张）。

The cost of moving grain food products was unchanged from May, but year over year are up 8%.

粮食产品的运输费用与5月份相比没有变化，但却比去年同期高8％。