التفاصيل البيبلوغرافية
| العنوان: |
Misdiagnosis of a cloacal exstrophy variant as urorectal septum malformation in a fetus by ultrasound: A case report. |
| المؤلفون: |
YANG-QING XU1, XIAO-HONG YANG1 yangxiaohong123@163.com, XIN-LIN CHEN1, XIU-QIIN JI1, SHENG ZHAO1 |
| المصدر: |
Experimental & Therapeutic Medicine. Aug2017, Vol. 14 Issue 2, p1665-1668. 4p. |
| مصطلحات موضوعية: |
*CLOACAL exstrophy, *UMBILICAL hernia, *BLADDER exstrophy, *SPINA bifida, *URINARY organ diseases |
| مستخلص: |
Cloacal exstrophy variants are comprised of a wide range of characteristics, of which there are four primary features, including omphalocele, bladder exstrophy, an imperforate anus and spina bifida. The existing literature regarding the differential diagnosis from alternative urinary diseases prenatally are limited. If the bladder is present, defects in the ventral wall may not be visualized with prenatal ultrasound in certain conditions, including oligohydramnios, and differential diagnosis from urorectal septum malformation sequence is a challenge. In order to improve the diagnosis of cloacal exstrophy variants, the present study investigated the misdiagnosis of a cloacal exstrophy variant as a urorectal septum malformation in a fetus by ultrasound and analyzed the reasoning of diagnosis in detail. [ABSTRACT FROM AUTHOR] |
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