遗传性

Cerebrotendinous xanthomatosis is a rare autosomal recessive disorder of bile acid synthesis, caused by impaired hydroxylation of cholesterol side chains due to deficiency of the mitochondrial enzyme sterol 27-hydroxylase （CYP27A1）, leading to accumulation of cholestanol and cholesterol in brain and other tissues.

文章摘要：脑腱黄瘤病是一种罕见的常染色体隐性遗传性胆汁酸合成障碍，由线粒体酶固醇27-羟化酶（CYP27A1）缺陷所致胆固醇侧链羟化受损引起，从而导致胆固烷醇和胆固醇在脑和其他组织贮积。

These cases included 55 cases of ITP,33 cases of HS,5 cases of MA,5 cases of PHT with splenic function accentuation,3 cases of splenic cyst,1 case of splenic abscess,3 cases of splenic angioma,2 cases of splenic angiolymphoma,2 cases of accessory spleen,and 1 case of splenic rupture.

病例构成为原发性血小板减少性紫癜(idiopathic thrombocytopenic purpura，ITP)55例，遗传性球形红细胞增多症（hereditary spherocytosis，HS）33例，地中海贫血(mediterranean anemia，MA)5例，肝硬化门脉高压脾亢5例，脾囊肿3例，脾脓肿1例，脾血管瘤3例，脾淋巴管瘤2例，副脾2例，脾破裂1例。

Alpha 1 - antitrypsin deficiency is an inherited disease that predisposes the affected person toemphysema, especially with smoking.

1型胰岛素缺乏症是种遗传性疾病，偏向发生于肺气肿的人身上，特别是

Michael Jackson was suffering from a rare genetic disease called Alpha-1 antitrypsin deficiency.

迈克尔杰苦卜患有一种罕见的遗传性疾病称为α- 1抗胰蛋白酶缺乏症。

Alpha-1 antitrypsin deficiency, hemochromatosis, Wilson's disease, galactosemia, and glycogen storage diseases are among the inherited diseases that interfere with the way the liver produces, processes, and stores enzymes, proteins, metals, and other substances the body needs to function properly.

阿尔法-1抗缺失，血色素、威尔森氏症、半乳糖、糖原贮藏疾病、遗传性疾病等方面的干扰肝脏产生方式、程序、商店、酵素、蛋白质、金属和其他物质的身体需要好好地运作。

Objective To analyse the mutation types of the NOTCH3 gene with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

目的 分析伴皮质下梗死及白质脑病常染色体显性遗传性脑动脉病的NOTCH3基因突变类型。

Objective To evaluate the peripheral neuropathy in patients with cerebral autosomal dominant arteriopathy with subeortieal infarcts and leukoeneephalopathy in respect of neurophysiology, neuropathology and possible mechanism.

目的报道常染色体显性遗传性脑动脉病伴皮质下梗死和白质脑病患者的周围神经电生理和病理改变特点。

Objective: In cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriolar walls are thickened with destruction of vascular smooth muscle cells and deposits of granular osmiophilic material.

目的：伴有皮层下梗死和脑白质病的常染色体显性遗传性脑动脉病的病理特征是血管损害，首先侵及中-小动脉，以血管平滑肌细胞变性为特征并可见嗜锇酸颗粒物质沉积。

The results showed that RAPD was used to determine the intraspecies or interspecies relationships among 8 isolates of Ascochyta from different origin.

对来自不同地域的8个Ascochyta 分离物进行RAPD分析，结果表明在种内，不同地域的Ascochyta遗传性具有一定的差异。

Because both intelligence and physical attractiveness are heritable, such assortative mating should create an extrinsic correlation between intelligence and physical attractiveness in the next generation.

由于这两个智力和身体吸引力是具有遗传性，这样选型交配应创造外在之间的智力和身体吸引力的相关性。

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％。