dystrophy的例句大全

Facioscapulohumeral muscular dystrophy ( FSHD) is a kind of progressive muscular disorder. It often occurs before 30 years old The face is initially involved, then the shoulder girdle, and finally the pelvic muscles Asymmetry of weakness is not unusual.

面肩肱型肌营养不良症（FSHD）是一种进行肌肉疾病，多于30岁以前发病，面肌总有受累；然后是肩肿带肌，能后是盆带肌等的萎缩和力弱。

Aim: To study the clinicopathologic manifestation of a pedigree of autosomal dominant benign congenital muscular dystrophy ( BCMD).

目的：对一良性先天性肌营养不良家系进行临床分析及肌活检组织学观察。

Formally known as "reflex sympathetic dystrophy," CRPS is a lifelong systemic disease which manifests itself as extreme burning pain, bone and skin changes, and unbelievable sensitivity to touch.

“CROS”的正式名称是“反射性交感神经营养障碍”，它是一种终身的系统疾病，表现为灼烧样剧烈疼痛，骨骼皮肤的改变，还有对触摸呈现难以置信的敏感。

Fixed dilated pupil after penetrating keratoplasty for macular corneal dystrophy and keratoconus

斑状角膜营养不良和圆锥形角膜行穿透性角膜移植术后固定瞳孔散大

Application of the Bgl ⅱ-Bln ⅰ dosage test to gene diagnosis of facioscapulohumeral muscular dystrophy 1A gene

BglⅡ-BlnⅠ剂量检测方法在面肩肱型肌营养不良症1A基因诊断中的应用

Clinical Analysis of Penetrating Keratoplasty Performed for Stromal Corneal Dystrophy

穿透性角膜移植术治疗基质层角膜营养不良临床分析

Research progress of molecular genetics of endothelial corneal dystrophy

角膜内皮营养不良分子遗传学研究进展

The clinical feature and surgical treatment for macular corneal dystrophy

斑状角膜营养不良的临床特征及手术治疗

Objective Molecular genetic analysis of a large Chinese corneal dystrophy kindred.

目的以基因突变分析一角膜营养不良家系的致病分子基础。

Molecular genetic study on patients with lattice corneal dystrophy in China

格子状角膜营养不良患者BIGH3基因突变的研究

Granular Corneal Dystrophy: A Case Report and Review of Literature

颗粒状角膜营养不良1例报告并文献复习

The useful information is provided from PCR-SSCP and sequencing for making gene diagnosis to corneal dystrophy.

PCR－SSCP结合DNA测序是检测BIGH3基因突变的简单、有效方法，有利于从分子学水平对角膜营养不良进行诊断分析，为优生优育及基因治疗提供依据。

By contrast, Simple leukoma, corneal dystrophy, corneal staphyloma had lower incidence.

单纯性角膜白斑、角膜营养不良、角膜葡萄肿的发生率较低。

Objective To report a large Chinese family with central areolar macular dystrophy and to identify its genetic entity by mutation analysis of candidate genes.

目的报道一个少见的中国人中心晕轮状黄斑营养障碍家系，通过候选基因突变分析探讨该家系发病的分子遗传学基础。

The Proportion and Clinical Feature of Duchenne Muscular Dystrophy With Autosomal Recessive Inheritance

常染色体隐性遗传的类Duchenne肌营养不良临床特征及其发生比率的估计值分析