• Another lasting symptom commonly is enamel hypoplasia.

    另一个持久症状通常牙釉质发育不全

    youdao

  • The purpose is to increase the corpus callosum hypoplasia CT performance.

    目的旨在提高胼胝体发育不全ct表现的认识。

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  • Objective To investigate the clinical character of congenital pulmonary hypoplasia.

    目的探讨先天性发育不全临床特征

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  • Congenital abnormalities - cerebellar hypoplasia, ocular defects, weak small calves.

    先天性畸形——小脑发育不全缺陷,牛犊弱小

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  • The anterior pituitary may be affected by absence or hypoplasia of the infundibulum.

    垂体前叶可以受累而缺失漏斗发育不良。

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  • Objective:To evaluate the sonographic features of hypoplasia of the right liver Lobe.

    目的探讨发育不良声像图特点

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  • The amplification of skull base by changing skull′s form decreased hypoplasia of mid-face.

    颅缝早闭症一定要扩大颅底才能彻底改变颅骨外形减少以后面部发育不良。

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  • As is implied by the name the most characteristic lesion is hypoplasia of the nasal turbinates.

    顾名思义,特征病变鼻甲发育不全

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  • As is implied by the name, the most characteristic lesion is hypoplasia of the nasal turbinates.

    顾名思义,特征病变鼻甲发育不全

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  • Objective: To investigate the value of diagnostic imaging for isolated right ventricular hypoplasia.

    目的探讨影像技术孤立性心室发育不全诊断价值

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  • GLUF has also been shown in mouse embryos to cause growth retardation increased death or hypoplasia.

    研究表明,草安造成小鼠胚胎发育迟缓、增加死亡或者发育不全。

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  • Purpose: To assess the diagnostic value of MRI and CAG in isolated right ventricular hypoplasia (IRVH).

    目的评价MRI诊断孤立心室发育不全(IRVH)价值与心血管造影(CAG)对比研究。

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  • Results The cause of congenital pulmonary hypoplasia may be related with heredity and virus infection early on fetus.

    结果先天性发育不全原因可能遗传胚胎早期病毒感染等因素有关。

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  • This child died soon after premature birth at 23 weeks gestation from pulmonary hypoplasia as a result of oligohydramnios.

    婴儿因羊水过少导致发育不良23早产死亡

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  • Conclusion there are the phenomena of hypoplasia in the gastrocnemius mep of the neonatal mouses with spina bifid a manifesta.

    结论显性脊柱仔鼠腓肠肌运动终板发育不全现象

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  • Results: The trisomy with cleft palate mouse foetuses had significantly developmental hypoplasia in the primary palatal shelves.

    结果模型虽无原发腭裂却伴有原发发育不足;

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  • The pathogenesis of them: in 3 cases were muscle fiber structure hypoplasia, 3 cases were arteriosclerosis and 1case was arteritis.

    病因有肌纤维结构发育不良3动脉粥样硬化3例、大动脉1

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  • The heart function of Scimitar syndrome should be followed-up for a long time for it usually associated with right lung hypoplasia.

    但弯刀综合征多伴右肺发育不良,心功能情况还长期随访

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  • Objective:To explore the value of bone marrow biopsy in diagnosing Myelodysplastic Syndrome(MDS) especially in the cases of MDS with hypoplasia.

    目的:评估骨髓活检骨髓增生异常综合征尤其是增生病例诊断价值

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  • Objective: to investigate the stability of internal midface distraction in correction of severe maxillary hypoplasia secondary to cleft lip and palate.

    目的:初步研究评价内置式牵引器牵引成骨治疗上颌发育不全术后稳定性

    youdao

  • Under light and electron microscope, it was seen that HCY 2 gene resulted in structure disturbance, endocardial cushion defect and hypoplasia of heart.

    HCY2基因引起心脏结构紊乱、心内膜缺损抑制心室心房发育,并可损害心肌细胞超微结构。

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  • METHODS: 3 children with hypoplasia of teeth were examined and analyzed carefully by clinical examination and laboratory test to find the genetic factors.

    方法采用临床实验室检查方法对3患儿进行详细体检分析导致出现牙根发育不良表型遗传学因素。

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  • It is a heterogeneous condition defined loosely by any combination of optic nerve hypoplasia, pituitary hypoplasia, and midline neuroradiological malformations.

    一种异质性条件界定任何视神经发育不全,垂体发育不良,畸形中线影像学结合松散

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  • This disease should be differentiated from variation of the large cisterna magna arachnoid cyst of the posterior forssa cystic neoplasm and severe hypoplasia of the cerebellum.

    本病后颅窝蛛网膜囊肿囊性新生物变异巨大大池以及重度小脑发育不全鉴别。

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  • Hypoplasia or absence of the major telencephalic commissures and a hypoplasia of corticospinal tracts to half the normal size, were the major neurodevelopmental defects we observed.

    我们观察到主要神经发育缺陷发育不全、或者缺失主要端脑连合处、皮质脊髓束因发育不全只有正常大小一半

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  • Focal dermal hypoplasia is a rare genodermatosis characterized by developmental defects of the skin, resulting in widespread linear lesions of dermal hypoplasia with adipose tissue in the dermis.

    局灶真皮发育不全综合征一种罕见遗传性皮肤病其特征是进行性皮肤缺失,引起真皮发育不全,出现线状皮损,真皮层可见脂肪组织

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  • Bone marrow hypoplasia coincided with the reduction of the ratios of granulocytes to erythrocytes as well as the megakaryocytes count. Conclusion Bone marrow biopsy and smear examination are valu

    苯中毒患者骨髓涂片粒红比值、巨核细胞数量随着骨髓增生程度降低而降低

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  • Bone marrow hypoplasia coincided with the reduction of the ratios of granulocytes to erythrocytes as well as the megakaryocytes count. Conclusion Bone marrow biopsy and smear examination are valu

    苯中毒患者骨髓涂片粒红比值、巨核细胞数量随着骨髓增生程度降低而降低

    youdao

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