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肌营养不良

n.Duchenne-Greisinger disease
网络DMD; muscular dystrophy; BMD

肌营养不良

英-汉网络释义

肌营养不良

DMD

假肥大肌营养不良(DMD)是一种X连锁隐性遗传病，一个女性的弟弟和舅舅都患DMD，试问这个家庭中谁肯定是携带者？谁可能 …

muscular dystrophy

首先，肌营养不良（muscular dystrophy）或者进行性肌营养不良（progressive muscular dystrophy）并不是一个单一的疾病实 …

BMD

关于假性肥大型肌营养不良(BMD)病情治疗DMD型肌营养不良如何用药我的儿子是肌营养不良吗？

muscular dystrophies

... Determination Analysis) 肌营养不良(Muscular Dystrophies) 肌萎缩脊髓性(Muscular Atrophy, Spinal) 移码突变(Frameshift M…

Duchenne

肌营养不良 (Duchenne 型) (Muscular dystrophy, Duchenne type)肌营养不良 (Emery-Dreifuss 型) (Muscular dystrophy, Emery-…

CMD

先天性肌营养不良（CMD）呈常染色体隐性遗传，包括一类出生时或出生几个月内出现肌无力和肌张力低，可伴有不同程度中 …

Duchenne muscular dystrophy

Duchenne型... ... ) Duchenne muscular dystrophy 肌营养不良症 ) Duchenne muscular dystrophy 肌营养不良 ) D/B MD 肌营养 …

dystrophin

...，与正常人有一定程度的重叠，准确可靠的诊断应来自对肌营养不良（dystrophin）基因分子水平的突变检测。

例句：

Duchenne Muscular Dystrophy (DMD) is one of the most common fatal genetic disorders to affect children around the world .

杜氏肌营养不良（DMD ）是最常见的致命的遗传疾病之一，影响到世界各地的儿童。

People with myotonic dystrophy have prolonged muscle tensing (myotonia) and are not able to relax certain muscles after use .

强直性肌营养不良病患具长期肌肉拉紧（肌强直）和在使用后无法放松某些肌肉。

It would not be suitable for treating different mutations in the dystrophin gene, or diseases not caused by nonsense mutations .

它对肌营养不良基因的其他类型的变异或非无意突变导致的疾病无效。

The mice showed a whole body effect , says Chamberlain, with a dramatic improvement of their dystrophy symptoms .

Chamberlain 说，老鼠全身戏剧性显示出了肌营养不良症状的改进效果。

She returned to movies in the early 2000s and played a woman with Muscular Dystrophy , which launched her superstardom .

而她重返影坛是在本世纪初，扮演一个患肌营养不良症的妇女，这个角色让她跻身巨星行列。

The drug , known as PTC124, has already had encouraging results in patients with Duchenne muscular dystrophy and cystic fibrosis .

被称为 PTC124 的药物，已经在治疗 Duchenne 肌营养不良和囊性纤维化的病人中获得了激动人心的成果。

Bell palsy (a type of neuritis ) paralyzes the muscles of one side of the face . Muscular dystrophy causes paralysis by attacking muscle.

贝尔氏麻痹（神经炎的一种）引起面部一侧的肌肉瘫痪。肌营养不良侵袭肌肉也能导致瘫痪。

The behavioral investigation on Duchenne muscular dystrophy animal model after marrow transplantation .

型肌营养不良模型鼠骨髓移植后的行为学观察。

ABSTRACT : Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).

摘要：目的探讨同患假肥大型肌营养不良症（DMD ）兄妹的临床以及实验室检查特点。

Muscular dystrophy is a group of more than 30 genetic diseases , characterized by progressive weakness and deterioration of skeletal muscles .

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。

Objective To perform early and presymptomatic diagnosis for facioscapulohumeral muscular dystrophy (FSHD).

目的对面肩肱型肌营养不良症（FSHD ）进行早期诊断和症状前诊断。

Objective To summarize the clinical characteristics of myotonic dystrophy (DM ).

目的总结强直性肌营养不良症（DM ）的临床特点。

Aim : To summarize the pathological characteristics of myotonic dystrophy (DM ).

目的：总结强直性肌营养不良（DM ）的肌肉病理特点。

Quick movements cause muscle stiffening. There is also a myotonic form of muscular dystrophy .

快速运动会引起肌强直，肌营养不良是另一种肌强直类型。

Specific muscle groups are affected by different types of muscular dystrophy .

特定的肌肉群受到不同类型的肌营养不良症。

The defective gene that causes Duchenne's and Becker's muscular dystrophies is located on the X-chromosome .

有缺陷的基因导致杜兴的和贝克尔的肌营养不良症是位于 X 染色体。

Muscular Dystrophy - Drug Pipeline Analysis and Market F. . .

肌营养不良症药品渠道分析及市场预测研究报告。

DMD is caused by a mutation of the gene for dystrophin, a protein in the muscles .

DMD 源于肌肉中一种称为肌营养不良蛋白的基因突变。

Most children with Duchenne muscular dystrophy die in their late teens or early 20s.

多数患进行性假肥大性肌营养不良的儿童可以活到十几岁或 20 几岁。

AVI-4658 is designed to benefit patients with certain mutations in the dystrophin gene .

4658 设计用于改善病人肌营养不良蛋白基因中的特定突变。

About 13 per cent of patients with Duchenne muscular dystrophy have a nonsense mutation and should respond to the drug .

大约有 13%的 Duchenne 肌营养不良病例是无意义突变，应该对该药有反应。

Objective: To find out the development of facioscapulohumeral muscular dystrophy in a large kindred over the past 20 years.

目的了解面肩肱型肌营养不良症一例大家系的发展形势，寻求防治方法。

The dystrophin gene is found on the X chromosome and passed on to children through a mother who is a carrier.

肌营养不良蛋白基因位于人类 X 染色体，携带基因突变的母亲会遗传给婴儿。

Over time it became apparent that a central player in myotonic dystrophy was RNA , a versatile molecule that is very similar to DNA .

随着时间推移，很明显 RNA 在强直性肌营养不良中起了核心作用，RNA 是一种类似于 DNA 普遍存在的分子。

AbstractObjectiveOur aim is to study the role of tissue inhibitor of metalloproteinase1 (TIMP1) in progressive muscular dystrophy (PMD ).

目的探讨金属蛋白酶组织抑制剂 1 （TIMP1 ）在进行性肌营养不良（PMD ）发病中的作用。

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