4.3 Article

Schinzel-Giedion syndrome

期刊

INTERNATIONAL JOURNAL OF UROLOGY
卷 8, 期 5, 页码 237-241

出版社

BLACKWELL SCIENCE ASIA
DOI: 10.1046/j.1442-2042.2001.00291.x

关键词

hydronephrosis; Schinzel-Giedion syndrome; urogenital anomalies

向作者/读者索取更多资源

A 2-month-old girl was brought to the Department of Pediatrics at Waltayama Rosai Hospital because of poor feeding since 1 month of age. She was the third child of young healthy nonconsanguineous parents whose first son was healthy but whose second son had died of 18 trisomy. Physical examination showed midfacial hypoplasia with coarse dysmorphic features, choanal stenosis, remarkable abdominal distention and bilateral talipes equivarus. Abdominal ultrasonography, computed tomography and drip infusion pyelogram showed left severe hydronephrosis and right moderate hydronephrosis. Having diagnosed Schinzel-Giedion syndrome, a left ureteroneocystostomy with tailoring was performed to preserve renal functions and to eliminate the urinary tract infection at the age of 3 months.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据