患者经常是又高又瘦的虚弱体型（“像马凡综合征”的外形），容易骨质舒松。
Individuals are often tall and slender with an asthenic habitus ("marfanoid" look) and prone to osteoporosis.
马凡综合征二尖瓣，见小叶增大，在左方远处的一个小叶向上隆起。
The mitral valve is shown in the same patient with Marfan's syndrome. The leaftlets of the mitral valve are redundant, and the one on the far left is ballooned upward.
经过粘蛋白染色的主动脉壁可见囊状中层坏死，这不仅是马凡综合征的表现，度且从动脉切面可见结缔组织薄弱，导致主动脉剥离。
This mucin stain of the wall of the aorta demonstrates cystic medial necrosis, typical for Marfan's syndrome and causes the connective tissue weakness that explains the aortic dissection.
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.
事发突然——因一种尚未确诊的疾病，疑似马凡氏综合征。
It was sudden - an undiagnosed disorder, a suspected case of Marfan syndrome.
目的观察马凡氏综合征心血管病变手术治疗效果。
Objective To observe the operative outcomes of Marfan's syndrome.
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 To summarize the experience of surgical treatment of ascending aortic aneurysm caused by Marfan syndrome and analyse related problems.
结果：马凡氏综合征主要累及骨骼、眼、心血管和神经系统。
Results: Marfan Syndrome affect mostly bone, eyes, circulatory system and nervous system.
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。
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。
Conclusions: The diagnosis of Marfan Syndrome depends on family histories, clinical features and laboratory results.
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