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- The inferior vena cava duplication is a rare congenital anomaly. 下腔静脉重复畸形是一种罕见的先天性血管发育变异。
- The blind-ending bifid ureter is a rare congenital anomaly of urinary system. 盲枝输尿管裂是一种极为少见的泌尿系统的先天异常。
- Patients with congenital anomaly of the inferior vena cava (IVC) usually lack clinical symptoms and signs. 下腔静脉之先天性异常一般缺乏临床症状,多为其他原因受检查而意外发现者。
- The em-embryology of IVC, causes of congenital anomaly and their clinical significance are discussed. 本文并讨论下腔静脉之胚胎演化,先天异常之成因,与其临床意义。
- Unilateral absence or hypoplasia of the pulmonary artery is an uncommon but not rare congenital anomaly. 摘要单侧肺动脉缺失或发育不全是一种先天性肺动脉发育异常。
- The etiologies of these lesions in the pancreatic head include inflammatory and infectious diseases, congenital anomaly, and lymphoproliferative processes. 这些胰脏头部伪肿瘤的形成原因包括了发炎性及感染性疾病,先天性异常及淋巴增生性疾病。
- Peripapillary staphyloma is a rare congenital anomaly and is even rare when it associated with serous retinal detachment. 摘要视乳头周围葡萄肿并发浆液性视网膜剥离,文献上只有一篇报告提及,但却未加以治疗。
- Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone. 摘要眼窝脑膜膨出是种罕见的先天性异常,其成因为头颅或眼窝骨的缺损使得脑脑从缺损处呈囊状的膨出。
- Retrocaval ureter is a rare congenital anomaly in which the ureter passes behind, and is compressed by, the inferior vena cava. 下腔静脉后输尿管为比较罕见之先天性异常,意指输尿管跑到下腔静脉后并被下腔静脉压迫。
- The presence of any congenital anomaly, abruption, and cord complications were associated with antepartum stillbirth in both races. 任何先天性畸形、胎盘早剥、脐带合并症是白人及非裔美国人发生产前死胎的危险因素。
- Lipomyelomeningocele is an uncommon congenital anomaly, resulting from outpouching of spinal cord and its surrounding leptomeninges through the bony defect of spina bifida. 脂肪脊髓脊膜膨出是一种罕见的先天异常,源于脊髓及脊膜经由脊柱裂而向外突出。
- Crossed renal ectopia is a rare congenital anomaly of the urinary tract, with an incidence of about one in 2000-7000 autopsies and a slight male predominance. 摘要当肾脏和输尿管进入膀胱不在身体的同一侧时,我们称之为跨越性异位肾脏。
- Poland's syndrome is a rare congenital anomaly characterized by deformities of the breast and chest wall that can be highly disfiguring in both men and women. 摘要波兰氏症候群是一种罕见的先天异常,它的特徵是乳房及胸壁的畸形,造成男性或女性患者外观上极大的影响。
- UAPA diagnosed in childhood usually has unilateral absence of the left pulmonary artery and associated congenital cardiovascular anomaly, while UAPA diagnosed in adult usually has UAPA on the right side without associated congenital anomaly. 儿童时期明确诊断的一侧肺动脉缺如多合并有心血管畸形 ,且左肺动脉缺如多见 ,成年人明确诊断的单发一侧肺动脉缺如多为右肺动脉缺如。
- The other minor congenital anomalies, such as preauricular sinus, undescended testis, chest wall anomaly are also investigated. 其他问题例如耳廓前窦,多汗症之调查结果亦可供儿童保健人员参考。
- This is a congenital anomaly that most often occurs in association with other anomalies or syndromes with specific genetic defects such as trisomy 18. 也可单独发生。
- congenital anomaly of reproductive system 生殖系统先天异常
- These anomalies were part of the polysplenia syndrome.Polysplenia syndrome is a rare congenital anomaly frequently associated with cardiopulmonary and abdominal disorders. 多脾症是一种罕见的先天异常,通常伴随心肺及腹部的问题,成人的病例通常只有轻微的异常。
- congenital anomaly of ocular muscle and tendon 先天性眼肌肌腱异常
- Congenital anomaly of aortic arch 先天性主动脉弓异常