Marfan

马凡氏

常用释义

马凡氏

扩展信息

马凡

A、大动脉炎又称马凡（Marfan）综合征B、是一种以大动脉中膜损害为主的非特异性全动脉炎 C、病理上，动脉全层呈弥漫或 …

马凡氏

马凡氏（Marfan ）综合征其为常染色显性遗传疾病。还有一些为多基因遗传性先天性心脏病。

马方

马方（Marfan）综合征是一种罕见的，导致眼、骨骼、心脏和血管异常的遗传性结缔组织疾病。马方综合征 - 症状马方综合征 - …

凡综合症

...确原因，但亦有部分患者本身身形较瘦长，或本身患上马凡综合症（Marfan）而先天性纤维组织有缺陷而令胸膜拉薄；也有 …

马方氏症

「马方氏症」（marfan）又称麻烦氏症，是一种大血管壁中层组织的退化性疾病，全身大血管都可能产生病变，但以升主动脉 …

马丸

...损、心室间隔缺损、法洛四联征、先天性肺动脉瓣狭窄、马丸（Marfan）综合征等。

马凡症

龟金国二下 (2011/06/29 08:55):【马凡症】(Marfan) *第15对染色体异常 *又高又瘦，深度的近视，眼内水晶体..观看完整全文…

例句

Conclusions: The diagnosis of Marfan Syndrome depends on family histories, clinical features and laboratory results.

结论：结合家族史、临床表现及有关的辅助检查可对马凡氏综合征作出诊断。

It 's vital that Marfan's be diagnosed as soon as possible, as the condition is commonly associated with weakness of the wall of the aorta.

马凡氏综合症要尽早发现，这至关重要，因为该病通常与主动脉的血管壁薄弱有关。

Marfan's Syndrome is a genetic disorder that affects the connective tissue in the body.

马凡氏综合症是基因型结缔组织病。

Objective Clinical symptom of Marfan syndrome and condition of undertaking ophthalmic surgery was researched.

目的探讨马凡氏综合征的临床表现及承受眼科手术的情况。

There was an inherited pattern for TAA in 21. 5 percent of non-Marfan patients.

在非马凡氏综合症胸主动脉瘤患者中，21.5%有遗传性。

This aortic dissection occurred just above the aortic root in a patient with Marfan's syndrome.

马凡综合征病人见主动脉根部上部发生剥离，主动脉向上撕裂。

Results: Marfan Syndrome affect mostly bone, eyes, circulatory system and nervous system.

结果：马凡氏综合征主要累及骨骼、眼、心血管和神经系统。

Methods The perioperative nursing care of 34 patients with lens dislocation subsequent to marfan's syndrome was studied retrospectively.

方法回顾性分析34例马方综合征晶体脱位围手术期护理方法。

Methods To observed the clinical data of 40 cases of Marfan syndrome.

方法对40例马凡氏综合征患者的临床资料进行回顾性分析。

Corrective effect of spinal three-dimensional orthopaedic internal fixation system on scoliosis of patients with Marfan syndrome

脊柱三维矫形内固定系统植入矫正马凡综合征患者脊柱侧凸的效应

Application of capsular tension ring during phacoemulsification for Marfan's syndrome complicated cataract with subluxated lens

囊袋张力环在马凡综合征超声乳化手术中的应用

Fibrillin-1 gene mutation in Chinese patients with Marfan syndrome and its gene diagnosis by haplotype analysis

马凡综合征微纤维蛋白1基因突变检测及单倍型连锁分析

The clinical manifestation and operative treatment for the scoliosis of Marfan's syndrome

马凡综合征脊柱侧凸的手术治疗

Central Pulse Pressure Is a Major Determinant of Ascending Aorta Dilation in Marfan Syndrome

中心脉压是马凡氏综合症升主动脉扩张的一个主要决定因子

Surgical Treatment for Cardiovascular Abnormalities Related to Marfan Syndrome

马凡综合征心血管病变的外科手术治疗

Iris hooks and modified capsular tension ring for subluxation lens in patients with Marfan's syndrome

虹膜拉钩联合可缝合囊袋张力环在马方综合征晶状体半脱位患者中的应用

Imaging diagnosis of cardiovascular lesions of Marfan syndrome

马凡综合征心血管病变的影像诊断

Molecular biological evolvement of Marfan syndrome

马凡综合征的分子生物学研究进展

Orthopedic procedure of scoliosis associated with Marfan's syndrome

马凡综合征合并脊柱侧凸的手术矫治

The clinical analysis of Marfan syndrome with aortic dissection

马方综合征并发主动脉夹层临床特征分析