| 释义 |
MarfanCOCA¹¹⁰⁸²⁶BNC²³⁶²¹³⁺¹
基本例句
🌏马凡；马凡氏；马方
Autopsy specimens of aortic dissecting aneurysm in17 cases were studied including11 cases with hypertension in the hypertension group and6 cases with Marfan's syndrome in the Marfan group.
对17例主动脉夹层动脉瘤的临床病理进行了分析。其中11例合并高血压高血压组；6例合并马凡氏综合征马凡氏组。 cnki
Background Progressive enlargement of the aortic root, leading to dissection, is the main cause of premature death in patients with Marfan's syndrome.
进行性扩张的主动脉根部导致的夹层是马凡综合症病人过早死亡的主要原因。 dxy
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。 yeeyan
The familial group was significantly younger than the sporadic group, but not as young as the Marfan group.
家族组明显比散发组年轻，但比马凡氏组年老。 dxy
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。 hicoo
Akhenaten's cone-shaped head, elongated face, fingers and toes, pot belly and flaring hips have led some scholars to suggest that he had hydrocephalus or Marfan's syndrome.
阿肯纳坦的头圆锥形，脸、手指和脚趾较常人略长，大腹便便，臀部肥大，这使得某些学者认为他曾得过脑积水。 hjenglish
Although the therapy for Marfan syndrome involves focusing specifically on the aortic root, any portion of the aorta is at risk for rupture or dissection as a consequence of its weaker nature.
虽然治疗马凡氏综合征只针对于主动脉根部，但主动脉瘤由于其较弱的特性任何部分都处于危险之中。 dxy
Conclusion Thoracic aortic aneurysm and aortic dissection over the40-year-old male with multiple, high blood pressure and Marfan syndrome as the main cause of morbidity;
结论胸主动脉瘤和主动脉夹层40岁以上的男性患者多发，高血压和马凡综合症为主要发病原因； fabiao
He ruled out speculation that Tutankhamun and his father suffered from“ Marfan syndrome” and another condition that could have led to enlarged breasts.
他排除了有关图坦卡蒙和他的父亲患有“马凡氏综合症”，以及另外一种可使胸部更丰满的病症的猜想。 www.chinadaily.com.cn
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。 yeeyan
Methods: To analyse the symptoms, physical characteristics, laboratory results and therapies in10 cases of Marfan Syndrome.
方法：对10例马凡氏综合征的症状、体征、辅助检查及治疗进行分析。 cnki
Methods The perioperative nursing care of34 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。211.151.93.212
Objective To observe the operative outcomes of Marfan's syndrome.
目的观察马凡氏综合征心血管病变手术治疗效果。 cnki
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。 dictall
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。 cnki
Objective:To discuss the characteristics of the Marfan syndrome with aortic dissectionAD.
目的：探讨马方综合征并发主动脉夹层临床特征。 cnki
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。 chemyq
Surgeries in16 cases 18 eyes of children Marfan's syndrome are reviewed.
报告16例18眼儿童马方综合征晶状体半脱位的手术治疗。 cnki
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。 dxy
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.
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。 com
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。 yeeyan |