This genetic disorder article is a stub.
这是一种遗传性疾病的文章作品。
Two of his grandchildren developed a rare genetic disorder, and one died.
他的两个孙儿得了一种罕见的遗传疾病，其中一个已经离开人世。
Marfan's Syndrome is a genetic disorder that affects the connective tissue in the body.
马凡氏综合症是基因型结缔组织病。
Narcolepsy affects about 1 in 2,000 people, and is thought to be a genetic disorder.
两千个人中就会有一个人得嗜睡症，并且通常认为嗜睡症是一种遗传疾病。
He had cardiovascular disease, some say. Or he had the rare genetic disorder Marfan's Syndrome.
他将会有天患有心血管疾病，他有罕见的遗传性疾病马凡氏综合症。
Huang Chuncai suffers from Neurofibromatosis, a rare genetic disorder that causes growth on nerve tissues.
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。
Tuberous sclerosis complex (TSC) is the most common genetic disorder associated with epilepsy and autism.
结节性硬化症是最常见伴有癫痫和自闭症的遗传性疾病。
About 100, 000 have retinitis pigmentosa, a progressive, genetic disorder that usually manifests in childhood.
而约有10万人患有视网膜色素变性疾病，它是一种进行性的遗传疾病，通常在儿童时期发病。
When patients have severe obesity from a young age, the possibility of a rare genetic disorder is much more likely.
儿童期起病的严重肥胖的患者，携带罕见的异常遗传基因可能性大大增高。
It is a love story about a man with a genetic disorder that causes him to time travel unpredictably, and about his wife, an artist.
这部电影讲述了一个由于遗传病而经常不可预知的在时间中穿梭的男子和他的艺术家妻子的爱情故事。
Some suspected substance abuse; last year a British journalist reported that Jackson had a genetic disorder that weakens the lungs.
一些人怀疑是药品滥用，就在去年，一名英国记者还报道说杰克逊有可以导致肺功能减弱的遗传性失调。
My wife and I chose to start funding these graduate students after we learned that our son has a rare, fatal genetic disorder.
自从得知我们的孩子得了一种罕见的，致命的遗传病后，我老婆开始资助生物学研究生。
If so, there could be a familial genetic disorder called fragile X, in which a certain portion of the X chromosome is abnormal.
如果有，那么你很可能有脆弱X基因的家族遗传病。也就是X基因的一部分是异常的。
The obstructive sleep apnea-hypopnea syndrome(OSAHS)is considered as a complex genetic disorder with high morbidity and mortality.
阻塞性睡眠呼吸暂停低通气综合征（OSAHS）是一种发病率高，危险性大的疾病。
In a new study, researchers propose that Henry had an X-linked genetic disorder and a rare blood type that could explain many of his problems.
在一项新研究中，科研人员推断亨利八世的X染色体遗传障碍和罕见血型是导致其状况频发的罪魁祸首。
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.
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。
Parents who have a family history of a severe genetic disorder use this test to determine the chances of the fetus developing a severe genetic disease.
一般有严重家族基因病史父母们用这项测试来检测胎儿患病的几率。
Scientists have taken a potentially important step toward a therapy for sickle cell disease, a common genetic disorder characterized by malformed red blood cells.
科学家可能已经取得了镰状贫血病治疗技术的一项重大进步。镰状贫血病是一种造成血细胞畸形的常见遗传病。
Scientists have taken a potentially important step toward a therapy for sickle cell disease a common genetic disorder characterized by malformed red blood cells.
科学家可能已经取得了镰状贫血病治疗技术的一项重大进步。镰状贫血病是一种造成血细胞畸形的常见遗传病。
Isolated case — an individual who is the only member of his or her kindred affected by a genetic disorder, either by chance or by new mutation. See also sporadic.
一个家系中唯一的患病个体，可由上代遗传基因决定，也可由于新突变产生。参见散发。
Tuberous sclerosis complex (TSC) is a genetic disorder that causes tumors to form in vital organs, primarily the brain, eyes, heart, kidneys, liver, lung and skin.
结节性硬化症（TSC）是一种遗传病，可导致脑、眼睛、心脏、肾脏、肝脏和皮肤等重要器官发生肿瘤。
Tuberous sclerosis complex (TSC) is a genetic disorder that causes tumors to form in vital organs, primarily the brain, eyes, heart, kidneys, liver, lung and skin.
结节性硬化症是一种遗传病，可导致脑、眼睛、心脏、肾脏、肝脏、肺和皮肤等重要器官发生肿瘤。
Several studies have shown that girls with a genetic disorder which exposes them to abnormally high prenatal levels of testosterone often develop boyish patterns of play.
几项研究表明，如果女孩因为遗传缺陷而在出生前受到高水平的激素影响，那么往往会出现男孩似的举动。
Conclusions: EBS-WC is an autosomal dominant genetic disorder with no special treatment. The diagnosis of this condition can be confirmed by the electron microscopy.
结论：EBS - WC主要是常染色体显性遗传性疾病，目前尚无有效的治疗方法，确诊需依靠电镜检查。
The unnamed patient suffers from an astoundingly rare genetic disorder called Urbach-Wiethe disease which has seen fewer than 300 reported cases since its discovery in 1929.
这位不知名的女士是一位极为罕有的乌-维氏病患者，这种病自1929年发现以来，有记实的患者不到300人。
Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.
一种遗传疾病，以先天性局部皮肤缺损、大疱性表皮松解症、口腔粘膜病变、甲营养不良为特征。
HEMOCHROMATOSIS - a genetic disorder involving increased absorption of iron by the gastrointestinal tract and deposition in the liver resulting ultimately in cirrhosis and liver failure.
血色沉着病——一种遗传性病症引起胃肠道吸收铁增多，沉积在肝脏，导致最终肝硬化或肝衰竭。
HEMOCHROMATOSIS - a genetic disorder involving increased absorption of iron by the gastrointestinal tract and deposition in the liver resulting ultimately in cirrhosis and liver failure.
血色沉着病——一种遗传性病症引起胃肠道吸收铁增多，沉积在肝脏，导致最终肝硬化或肝衰竭。
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