【佳学基因检测】做尿囊性腹壁缺损基因检测需要多少钱

基因检测导读：

尿囊性腹壁缺损是佳学基因疾病表征、影响生活质量的一种异常生命活中现象。解决或者是消除尿囊性腹壁缺损对生理活动影响的一个方式是找到导致尿囊性腹壁缺损出现的原因。尿囊性腹壁缺损基因检测，尤其是在基因解码技术支持下的基因信息分析，可以厘清尿囊性腹壁缺损是由基因位点突变引起的，还是由环境及生活习惯的影响产生的。原因不同，其持续的时间会不同，对健康的影响深度也不一样。佳学基因尿囊性腹壁缺损基因检测在大理白族自治州精准医医学中心小规模推广后，快速得到大家认可，同远盟健康基因检测费用一样成为大家关注的焦点。

本文关键词

尿囊性,腹壁,缺损,靶向,费用,基因检测

人体疾病表征数据库查询

产生尿囊性腹壁缺损医师会怀疑以下疾病类型：

怎样才能诊断准确？

HP:0030733

表型描述

An abdominal wall defected related to a developmental anomaly of the allantois, which is an embryonic structure that develops as a diverticulum off the yolk sac at about 16 days post fertilization. During further development, the allantois becomes incorporated into the body of the embryo, connecting the ventral aspect of the urogenital sinus (which will develop into the upper pole of the urinary bladder) to the external portion of the umbilicus. Upon further development, the lumen of the allantois becomes obliterated and forms a thick fibrous cord called the urachus, which connects the apex of the bladder to the umbilicus. In adults, the urachus is known as the median umbilical ligament. Failure of the allantoic cavity to obliterate can result of one of four conditions: 1) congenital patent urachus (a completely open connection between bladder and umbilicus); 2) vesicourachal diverticulum (a diverticulum off the bladder but not communicating with the umbilicus); umbilical cyst and sinus (not communicating with the bladder); and 4) alternating urachal sinus. An abdominal wall defect can be associated with a urachal cyst.