- 更多网络例句与旋转不良相关的网络例句 [注：此内容来源于网络，仅供参考]
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Conersely, mutations in genes that adersely affect both respiratory and embryological nodal cilia are a significant cause of heterotaxy and congenital heart disease, and screening for PCD is indicated in those patients.
相反地，对呼吸和胚胎学的交点纤毛产生不良影响的基因突变是引起心脏旋转不良和先天性心脏病的重要原因，在那些病人中表现为PCD。
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Results: The bleeding site: in 136 cases, 66 cases of upper gastrointestinal bleeding (48.5%), 42 cases of lower gastrointestinal bleeding (31%), all 28 cases of gastrointestinal bleeding (20.5%); bleeding: 34 cases of bleeding ( 25%), amount of bleeding in 70 cases (51%),32 cases of heavy bleeding (24%); the cause of bleeding: 87 cases of stress ulcer (64%), neonatal necrotizing enterocolitis 25 cases (18%), 16 cases of neonatal hemorrhagic disease (12%), intestinal malrotation volvulus merge two cases (1.5%) and stomach wall muscle dysplasia and 2 cases (1.5%), 4 cases of unknown causes (3%); Treatment Results: 129 cases of cure (95%), the death of 4 (3%), three cases of auto-discharge (2%).
结果：出血部位：136例中，上消化道出血66例（48.5％），下消化道出血42例（31％），全消化道出血28例（20.5％）；出血量：少量出血34例（25％），中量出血70例（51％），大量出血32例（24％）；出血的病因：应激性溃疡87例（64％）、新生儿坏死性小肠结肠炎25例（18％）、新生儿出血症16例（12％）、肠旋转不良合并肠扭转2例（1.5％）和胃壁肌层发育不良2例（1.5％），原因不明4例（3％）；治疗结果：治愈129例（95％），死亡4例（3％），自动出院3例（2％）。
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Twele patients with heterotaxy had cardiac and/or ascular abnormalities, and most (8 of 12 patients) had complex congenital heart disease.
12名有心脏旋转不良患者有心脏/血管异常，并且大多数(8 /12名患者)有复杂先天性心脏病。
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Conclusions— At least 6.3% of patients with PCD hae heterotaxy, and most of those hae cardioascular abnormalities.
至少6.3%的PCD患者伴有心脏旋转不良，并且大多数还伴发有心血管异常。
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Situs solitus and situs inersus totalis were identified in 46.0% and 47.7% of patients, respectiely, and 6.3%(21 patients) had heterotaxy.
心房正常位和心房反位各占了在46.0%和47.7%， 6.3%(21名患者)有心脏旋转不良。
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Background— Primary ciliary dyskinesia is a recessie genetic disorder that is characterized by sinopulmonary disease and reflects abnormal ciliary structure and function. Situs inersus totalis occurs in 50% of PCD patients (Kartagener's syndrome in PCD), and there are a few reports of PCD with heterotaxy, such as cardioascular anomalies.
背景 先天性纤毛运动异常症是以呼吸道感染和纤毛结构与功能不正常为特征的隐性遗传性疾病。50% PCD患者易发生完全性内脏异位(如PCD中的Kartagener综合征)，有小部分PCD伴有心脏旋转不良等心血管异常现象。
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The prealence of congenital heart disease with heterotaxy is 200-fold higher in PCD than in the general population (1:50 ersus 1:10 000); thus, patients with PCD should hae cardiac ealuation.
在PCD中先天心脏病伴发心脏旋转不良发生率比在总人口中高出200倍(1 ：50对1：10 000)；因此，对PCD患者应该进行心脏病评估。
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Baby two years old my family that much, but often this happens, I also go to hospital from her reading, but also consulted the Doctor, general lead to a child has a stomachache so several reasons: one, intestinal cramps. 2, intestinal parasitic diseases. 3, mesenteric lymphadenitis, appendicitis, diverticulitis Meikle. 4, congenital malrotation. 5, inguinal hernia, internal hernia (diaphragmatic hernia, obturator hernia) 6, intussusception, volvulus.
我家孩子两周岁多，也常有这种情况发生，我也特意去医院领她看过，也咨询过医生，一般引发宝宝子肚子疼的原因有这么几种：1、肠痉挛。2、肠寄生虫病。3、肠系膜淋巴结炎、阑尾炎、米克尔憩室炎。4、先天性肠旋转不良。5、腹股沟疝、内疝6、肠套叠、肠扭转。
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ABSTRACT Objective: To discuss the X-ray feature of intestinal malrotation with midgut volvulus and its diagnostic value.
目的：评价腹部平片对婴儿肠旋转不良合并中肠扭转的诊断价值。
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Objective To research the diagnosis and treatment of congenital malrotation of the intestine.
目的 探讨先天性肠旋转不良的诊断及治疗方法我院从1978年1月—2007年2月手术治疗先天性肠旋转不良91例，平均年龄11.3 月（2天～13岁）。
- 更多网络解释与旋转不良相关的网络解释 [注：此内容来源于网络，仅供参考]
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malt sugar：饧
malrotation 旋转不良 | malt-sugar 饧 | maltase 麦芽糠酶
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malposed tooth：错位牙,逆生牙
Malpighian stratum 马耳皮基氏层 | malposed tooth 错位牙,逆生牙 | malrotation of intestine 肠旋转不良
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malrotation：旋转不良
1,小肠扭转很多是由于胚胎期中肠(midgut)发育过程中旋转不良(malrotation). 1,小肠扭转很多是由于胚胎期中肠(midgut)发育过程中旋转不良(malrotation). 1932年: Ladd 发表了肠旋转不良(malrotation)十二指肠梗阻及外科处理. 至今方法无大的变化.
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renal malrotation：肾旋转不良
肾轴性旋转 axial rotation of kidney | 肾旋转不良 renal malrotation | 巨肾盏 megacalycosis; megacalyx
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malrotation of intestine：肠旋转不良
先天性肠旋转不良(malrotation of intestine)是由于胚胎发育中肠管旋 转发生障碍, 从而并发肠梗阻或肠扭转.