It was sudden - an undiagnosed disorder, a suspected case of Marfan syndrome.
事发突然——因一种尚未确诊的疾病，疑似马凡氏综合征。
Adsorption of copper cation from aqueous solution by Marfan stone has be studied.
研究了麦饭石对水溶液中铜离子的吸附作用。
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。
Objective: To discuss the characteristics of the Marfan syndrome with aortic dissection (AD).
目的：探讨马方综合征并发主动脉夹层临床特征。
Ambassador to the Malaysian side in Malaysia to negotiate, requiring Marfan to carry out search and rescue work.
驻马来西亚大使向马方提出交涉，要求马方全力开展搜救工作。
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。
Early diagnosis and advances in medical care have greatly improved the quality and length of life for people with Marfan syndrome.
马凡氏症的早期诊断以及护理技术的进步大大地提高了患者的生活质量和寿命。
Objective To summarize the experience of surgical treatment of ascending aortic aneurysm caused by Marfan syndrome and analyse related problems.
目的总结马凡氏综合征所致升主动脉瘤手术治疗的经验，并分析探讨其相关问题。
Objective:Mindless diagnosis of Marfan syndrome should be avoided, because its clinical management and genetic consultation are different from other diseases.
目的：由于马方综合征的临床处理与遗传咨询和其它疾病截然不同，因此应尽量避免滥诊和误诊。
Abstract : Objective To detect FBN1 mutation by screening FBN1 gene from 4 patients with Marfan syndrome(MFS)to investigate the correlation between the gene mutation and the MFS.
摘要 ：目的对4例汉族马凡综合征（MFS）患者的原纤蛋白-1（FBN1）基因进行突变筛查，探讨MFS与FBN1基因突变的关系。
Abstract : Objective To detect FBN1 mutation by screening FBN1 gene from 4 patients with Marfan syndrome(MFS)to investigate the correlation between the gene mutation and the MFS.
摘要 ：目的对4例汉族马凡综合征（MFS）患者的原纤蛋白-1（FBN1）基因进行突变筛查，探讨MFS与FBN1基因突变的关系。
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