双子宫伴梗阻性半阴道及肾缺如：磁共振成像表现
Uterus didelphys with obstructed hemivagina and renal agenesis: MRI findings.
作者信息
Talebian Yazdi A, De Smet K, Ernst C, Desprechins B, de Mey J
机构信息
Department of Radiology, University Hospital Brussels, UZ Brussel, Brussels, Belgium.
出版信息
JBR-BTR. 2011 Jan-Feb;94(1):16-8. doi: 10.5334/jbr-btr.475.
PMID:21466056
Abstract
Müllerian duct abnormalities (MDA) are developmental disorders leading to dysmorphism of the female genital tract. Currently the Buttram and Gibbons classification of these entities is widely used. We present a case of a young girl with uterus didelphys and ipsilateral renal agenesis.
摘要
苗勒管异常（MDA）是导致女性生殖道畸形的发育障碍。目前，这些实体的巴特拉姆和吉本斯分类被广泛使用。我们报告一例患有双子宫和同侧肾缺如的年轻女孩病例。
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