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是否尿直肠隔序列畸形是脊椎骨缺损、肛门闭锁、气管食管瘘、肾脏缺损和桡骨发育不良综合表现的另一种表现:1例病例报道及文献回顾
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作者 c.ien J.-c. tiu c.-m. +1 位作者 D.-m. Niu 贺莉 《世界核心医学期刊文摘(儿科学分册)》 2005年第11期41-41,共1页
The urorectal septum malformation sequence (URSMS) consists of multiple systems anomalies including ambiguous genitalia, the absence of a perineal opening, an imperforate anus, and urogenital, colonic and lumbosacral ... The urorectal septum malformation sequence (URSMS) consists of multiple systems anomalies including ambiguous genitalia, the absence of a perineal opening, an imperforate anus, and urogenital, colonic and lumbosacral anomalies. We describe a 3-day-old female infant with characteristic URSMS and review its clinical manifestations, outcomes and putative pathogenesis. We also compare its characteristics with those of the vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia (VATER) association. Conclusion: Although defects of the urorectal septum malformation sequence and the vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia association overlap, we believe that they are separate entities. Differentiating the urorectal septum malformation sequence from vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia association is helpful to develop appropriate clinical investigations and search for the aetiology and pathogenesis of these diseases. 展开更多
关键词 尿直肠隔 肛门闭锁 气管食管瘘 骨缺损 发育不良 文献回顾 泌尿生殖器 临床调查 发病机制 缺如
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