结果本组粘连性肠梗阻的病因包括手术后粘连22例、腹部慢性炎症粘连5例、先天性发育异常1例。
Retults In the group, there were abdominal operation previously in 22 cases, acute or chronic inflammation of abdomen in 5 cases, and congenital intestinal obstruction in 1 case.
圆锥角膜是一种先天性发育异常，是一种以角膜扩张为特征，致角膜中央部向前凸出、变薄呈圆锥并产生高度不规则散光的角膜病变。
Keratoconus is an uncommon autosomal recessive inheritance, characteristic of corneal ectasia, which results in the corneal central anterior bulging, conus formation and high irregular astigmatism.
尽管研究人员已经对房室间隔发育的基因控制有了很多认识，但目前还没有确定是哪种基因异常引起房室间隔相关的先天性心脏缺损。
Despite extensive knowledge of the genetic control of AVS development, few genetic lesions have been identified that are responsible for AVS-associated congenital heart defects.
本报告认为该肾动脉肌纤维发育异常是后天的，可能不是先天性的。
The report suggests that fibromuscular dysplasia of the renal arteries is acquired and may not be presented from birth.
先天性耳前瘘管由胚胎发育异常引起。
Congenital preauricular fistula is a common abnormality consequent on deficiency of embryonal development.
先天性小眼球是一种先天发育异常性眼科疾病，遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。
Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
先天性小眼症是在胚胎发育早期眼球生长停滞所造成的先天异常。
Congenital microphthalmos is a rare ocular anomaly due to arrest of ocular growth and development in early fetal life.
胎儿时期心脏血管发育异常而致的心脏和心脏大血管畸形称先天性心脏病(CHD)。
Abnormal development of heart and blood vessels in embryo with the result that defect of heart and cardiac vessels is called congenital heart disease (CHD).
许多技术已被应用于颅颈交界处和寰枢椎来解决儿童的先天性或发育性异常。
Summary of Background Data. Surgeons have applied several techniques for craniocervical and atlantoaxial spondylodesis to address congenital or developmental abnormalities in children.
她患有苯丙酮酸尿症，这是一种先天性代谢异常病，会影响大脑发育、损伤脑部神经和损害智力。
Borsi Batki suffers from phenylketonuria (PKU), a metabolic disorder that if undetected, can lead to problems with brain development, progressive mental retardation, brain damage and seizures.
其发生青光眼的机制与虹膜前房角的发育异常有关。对先天性葡萄膜外翻合并青光眼的患者应尽早发现，早期干预和治疗。
The pathogenesis of secondary glaucoma is related to iridotrabecular dysgenesis. It is essential to detect and to treat the secondary glaucoma as early as possible.
其发生青光眼的机制与虹膜前房角的发育异常有关。对先天性葡萄膜外翻合并青光眼的患者应尽早发现，早期干预和治疗。
The pathogenesis of secondary glaucoma is related to iridotrabecular dysgenesis. It is essential to detect and to treat the secondary glaucoma as early as possible.
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