脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。
Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.
化综合征是一种X连锁的隐性遗传病，为男性假两性畸形中最常见的类型。
Testicular feminization syndrome, the most common type of male pseudohermaphroditism, is an X-linked recessive disorder.
遗传性无纤维蛋白原血症是一种由于纤维蛋白原基因缺陷所致常染色体隐性遗传病。
Congenital afibrinogenemia is a rare autosomal recessive disorder, characterized by the complete absence or extremely reduced level of fibrinogen.
毫不奇怪，有家族性遗传病病史的成员，已经开始像害怕疾病本身一样害怕基因检查。
Not surprisingly, people from high-risk families have come to fear tests almost as much as the disease.
没有关于一个人类被迫保持不睡的时间久到死亡的记录，但是有一种叫做致命性家族失眠症的遗传病似乎表明人类无睡眠时间是有极限的。
There are no records of a human having been intentionally kept awake long enough to kill them, but a hereditary disease called fatal familial insomnia suggests there is an ultimate limit.
在发达国家，它已经证明了在血友病等疾病的突破性治疗以及检测遗传病的技术方面具有价值。
In the developed world, it has already proved its worth in groundbreaking treatments for diseases such as haemophilia, and techniques for detecting genetic diseases.
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.
我有家族性的心脏病遗传病史。
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。
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.
结论sle具有多基因遗传病的特点，遗传因素在决定sle的易患性上起到重要的作用。
Conclusions SLE has characteristics of polygenic disease. Genetic factor might play an important role in the liability of SLE.
限制性酶切片段长度多态性（RFLP）作为共显性的遗传标记，已广泛应用于遗传病的产前诊断。
As a codominant genetic marker, restriction fragment length polymorphisms, referred as RFLPs, has been widely Applied to the prenatal diagnosis of some genetic diseases.
将特异的干细胞注入患有遗传病的狗血流后，这种病可以导致进行性瘫痪。他们发现狗的情况得到改善。
After transfusing a specific type of stem cell into the bloodstream of dogs with the genetic disease that causes progressive paralysis, they found improvements in the animals.
WD是少有的可用药物治疗的遗传病，但未经合理的治疗后果往往是致命性的。
WD is a drug-treatable hereditary disease, which is rare. However without reasonable treatment, outcome is often fatal.
是否有一种遗传病：“综合性并发症”它是一种什么样的病呢？
Whether to have a kind of hereditary disease: "Omnibus complication" a kind of what kind of disease is it?
是否有一种遗传病：“综合性并发症”它是一种什么样的病呢？
Whether to have a kind of hereditary disease: "Omnibus complication" a kind of what kind of disease is it?
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