1) limb-girdle muscular dystrophy type 2B
肢带型肌营养不良2B型
1.
Clinical and pathological features of limb-girdle muscular dystrophy type 2B;
肢带型肌营养不良2B型的临床和病理特点
2) limb-girdle muscular dystrophy 2B
肢带2B型肌营养不良
1.
Dysferlin deficiency: the cause of limb-girdle muscular dystrophy 2B and Miyoshi myopathy in a Chinese pedigree;
Dysferlin缺陷:肢带2B型肌营养不良与Miyoshi肌病的致病原因
3) 1imb-girdle muscular dystrophy/diagnosis
肢带型肌营养不良/诊断
4) limb-girdle muscular dystrophy
肢带型肌营养不良
1.
Exclusive gene mapping on limb-girdle muscular dystrophy in a Chinese kindred;
肢带型肌营养不良一家系致病基因排除性定位
2.
Objective:To analyze the clinical and electrophysiological features of one genealogy with limb-girdle muscular dystrophy(LGMD).
目的分析肢带型肌营养不良(limb-girdle muscular dystrophy,LGMD)家系的临床与电生理特点。
5) Duchenne muscular dystrophy
Duchenne型肌营养不良
1.
In this article,the procedures and techniques of PGD for Duchenne muscular dystrophy are summarized,and a discussion will be developed on the existing problems,solutions and its application prospects.
总结Duchenne型肌营养不良症植入前遗传学诊断的步骤和各项技术,并对其目前存在的问题和解决方法以及其应用前景进行讨论。
6) Duchenne muscular dystrophin (DMD)
Ducheune型肌营养不良
补充资料：眼肌型进行性肌营养不良
眼肌型进行性肌营养不良
又称Kilon与Nevin型"肌营养不良。散发，呈常染色体显性遗传。20岁左右起病。缓慢进展的二侧眼睑下垂，眼球运动障碍，导致眼球固定。诊断较困难，若同时伴有肢体近端肌或口周部肌病症者，有助诊断。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条