那是一种遗传性疾病。
这是一种遗传性疾病的文章作品。
肌阵挛癫痫常为一种遗传性疾病，可有家族遗传史。
Myoclonic epilepsy is a genetic disease often can be a family history.
色盲是一种遗传性疾病，由于色觉机理尚未研究清楚，一向不能矫治。
Color blindness, a kind of inheritance diseases, has been always believed as an untreated disease, because the mechanism of color vision has been unknown.
戈谢病是一种遗传性疾病，是由缺乏一种名为葡萄糖脑苷脂酶的酶引起的。
Gaucher disease is an inherited disorder that is caused by a deficiency in an enzyme called glucocerebrosidase.
乳糜泻是一种遗传性疾病，它能损害小肠功能，干扰食物中营养物质的吸收。
Celiac disease is a genetic autoimmune disorder that damages the small intestine and interferes with absorption of nutrients from food.
结论：家族性结肠息肉病是一种遗传性疾病，癌变率较高，早期诊断、合理治疗可以取得满意的疗效。
Conclusions: FPC is a kind of hereditary diseases which has a high cancerization rate; there is satisfactory result when early diagnosis and reasonable treatment are applied.
TSC是一种遗传性疾病，导致良性肿瘤的形成，在许多不同的器官，主要是在脑部，眼睛，心脏，肾脏，皮肤和肺部。
TSC is a genetic disorder that causes benign tumors to form in many different organs, primarily in the brain, eyes, heart, kidney, skin and lungs.
黄春才所患的肿瘤是神经纤维瘤，属于一种罕见的遗传性疾病，肿瘤组织为快速生长的神经组织。
Huang Chuncai suffers from Neurofibromatosis, a rare genetic disorder that causes growth on nerve tissues.
两种普通药对实验老鼠的早衰症有效，而早衰症是是一种罕见的遗传性疾病。
TWO common drugs have reversed the effects in mice of progeria, a rare genetic disease that causes premature ageing.
结节性硬化是一种常染色体显性遗传性疾病。过去临床上主要靠病人有癫痫、智力低下和皮脂腺瘤三大体征来诊断。
Tuberous sclerosis (TS) is an exceptional chromosomal inherited disease, This disease was mainly diagnosed by three clinical appearances: epilepsy, intellectual disturbance, and sebaceous adenoma.
它已经是一种标准的临床实践，用于检测35岁以上的妇女或者有某种遗传性疾病的妇女。
It has been a standard clinical practice to test women using this procedure who are 35 years or older as well as women who are genetically predisposed for certain disorders.
囊性纤维变性是一种严重的遗传性疾病，影响小渠道，使营养物质进出细胞。
Cystic fibrosis is a serious inherited disease that affects tiny channels that bring nutrients into and out of cells.
原发性高血压是一种遗传素质与环境因素相互作用所导致的多基因遗传性疾病。
Human essential hypertension is a complex polygenetic disorder which is thought to be determined by complex interactions between genetic predisposition and environmental factors.
约4%的新生儿受一种或多种先天性疾病的影响，在所有的先天性疾病中大约35%为遗传性疾病。
About 4 percent of newborn bodies are affected by one or more kinds of congenital diseases. And, there are about 35 percent of congenital diseases belong to inherited diseases.
神经鞘脂病是一类神经鞘脂分解代谢障碍的遗传性疾病，酶学检测是确诊的一种主要手段。
Sphingolipidosis is a group of hereditary diseases characterised by the deficiency in enzymes responsible for catabolism of sphingolipids.
肌营养不良是30种遗传性疾病的一种，以骨骼肌进展性无力和变性为特点。
Muscular dystrophy is a group of more than 30 genetic diseases, characterized by progressive weakness and deterioration of skeletal muscles.
基因治疗是一种新的治疗手段，可以治疗多种疾病，包括癌症、遗传性疾病、感染性疾病、心血管疾病和自身免疫性疾病。
Gene therapy is a new therapeutic tool for the treatment of diverse types of diseases, including cancer, congenital genetic, infectious, cardiovascular and autoimmune diseases.
强直性肌营养不良症为一种少见的多系统受累的遗传性疾病。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
强直性肌营养不良症为一种少见的多系统受累的遗传性疾病。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
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