Unfortunately, there are no great treatments for Duchenne or Becker muscular dystrophy.
DMD或BMD暂时没有好的治疗方法。
单词 | Becker muscular dystrophy |
释义 |
Becker muscular dystrophy
原声例句
Osmosis-肌骨 Unfortunately, there are no great treatments for Duchenne or Becker muscular dystrophy. DMD或BMD暂时没有好的治疗方法。 Osmosis-肌骨 Since this is linked to the X chromosome, both Duchenne and Becker muscular dystrophy are called X-linked recessive. 由于发病与X染色体有关联,DMD和BMD被称为X连锁隐性遗传。 Osmosis-肌骨 Now, the fact that both Duchenne and Becker muscular dystrophy result from mutations in the same dystrophin gene means that they are " allelic disorders, " DMD和BMD都是由于同一抗肌萎缩蛋白基因突变引起的,意味着二者是“等位基因疾病”。 Osmosis-肌骨 Within that group, dystrophinopathies are the most common, which includes Duchenne muscular dystrophy, or DMD, and Becker muscular dystrophy, both of which result from mutations in the dystrophin gene. 这些功能紊乱中,营养不良疾病是最常见的,包括Duchenne型肌营养不良(DMD)和Becker型肌营养不良(BMD);这二者都是由抗肌萎缩蛋白基因突变导致的。 Osmosis-肌骨 On the other hand, mutations that allow for a misshapen protein to form, like missense mutations, lead to Becker muscular dystrophy which is basically a milder form of Duchenne muscular dystrophy that presents later on, usually between age 10 to 20. 另一方面,突变(如错义突变)会导致畸形蛋白形成,引发BMD,病情比DMD较轻,发病年龄较晚,一般在10到20岁。
中文百科
贝克型肌肉萎缩症 Becker's muscular dystrophy(重定向自Becker muscular dystrophy)
贝克型肌肉萎缩症是肌肉萎缩蛋白缺陷造成的疾病,患者可以制造肌肉萎缩蛋白,但功能不正常且无法百分之百有效工作。虽与杜兴氏肌肉营养不良症有相同的基因缺陷,但表现型有所不同,此症患者病症通常较轻微。裘馨氏肌肉萎缩症的肌肉萎缩蛋白是完全缺陷,而此症的肌肉萎缩蛋白只是部分缺陷。 其发生率为1/30000,发病年龄平均为11岁。 遗传方面,其遗传方式为一种X染色体性联隐性遗传的进行性肌肉萎缩症,女性通常只会是隐性带因者。
英语百科
Becker's muscular dystrophy 贝克型肌肉萎缩症(重定向自Becker muscular dystrophy)
![]() ![]() Becker muscular dystrophy is an X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis.It is a type of dystrophinopathy. This is caused by mutations in the dystrophin gene, which encodes the protein dystrophin. Becker muscular dystrophy is related to Duchenne muscular dystrophy in that both result from a mutation in the dystrophin gene |
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