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作者:Rajendran Ramaswamy , Rayan Ahmed Baz , Marwan Alchami ...
来源:[J].Pediatric Urology Case Reports, 2019, Vol.6 (4), pp.88-94
摘要:Absence of any orifice in perineum, presence of smooth perineum, and absence external genitalia are characteristic of cloacal dysgenesis sequence (CDS). Newborn of 40w gestational age, born to mother with oligohydramnios, had very low APGAR scores, and was put on ventilator. Chil...
作者:G. Wagner , A. Holschneider , M. Gharib
来源:[J].Eur J Pediatr Surg(IF 0.839), 1998, Vol.8 (3), pp.182-185
摘要:Cloacal malformations are rare, complex inhibitional anomalies of early embryogenesis. We report a patient with a cloacal malformation in which a septate vagina and a rectal fistula emptied through a common orifice onto an exstrophic bladder plate. Additional anomalies included a...
作者:Cecile Colpaert , Johannes Bogers , Koen Hertveldt ...
来源:[J].Pathology - Research and Practice(IF 1.213), 2000, Vol.196 (11), pp.783-790
摘要:... Three fetuses showed an abdominal wall defect with eventration of abdominal organs, cloacal exstrophy, absent external genitalia, abnormal internal genitalia, scoliosis and lower limb defects. One fetus showed failure of closure of both thoracic and abdominal walls with ectop...
作者:Ramaswamy Rajendran Baz Rayan Ahmed Alchami Marwan Mukattash Ghazi pediatric surgery
来源:[J].Pediatric Urology Case Reports, 2019, Vol.6 (4)
摘要:Absence of any orifice in perineum, presence of smooth perineum, and absence external genitalia are characteristic of cloacal dysgenesis sequence (CDS). Newborn of 40w gestational age, born to mother with oligohydramnios, had very low APGAR scores, and was put on ventilator. Chil...
作者:Yui Kinjo , Hitoshi Masamoto , Hayase Nitta ...
来源:[J].Case Reports in Obstetrics and Gynecology, 2018, Vol.2018
摘要:... the fetus showed fused lower limbs, bulging abdomen, and absent external genitalia and was diagnosed with type III sirenomelia. On autopsy, no normal bladder was observed, but duodenal atresia, anorectal atresia, and right renal agenesis were found. An intra-abdominal cyst, d...
作者:Joseph R. Siebert , Joe C. Rutledge , Raj P. Kapur
来源:[J].Pediatric and Developmental Pathology(IF 0.859), 2005, Vol.8 (3), pp.339-354
摘要:... We present 2 representative cases, a 19-week-old female fetus with duplication of several caudal structures and a 21-week-old male fetus with cloacal exstrophy variant and demised co-twin with lower abdominal wall defect, extruded intestinal tract, absent external genitalia, ...
作者:I. V. Meisheri , V. S. Waigankar , M. P. Patel ...
来源:[J].Pediatric Surgery International(IF 1.216), 1996, Vol.11 (8), pp.580-581
摘要:... We present another case of this fascinating anomaly with fused lower limbs, absent external genitalia, and absent genitourinary system. The patient could not be salvaged because of bilateral renal agenesis. Detailed autopsy findings and a review of the literature are presente...
作者:Guido Currarino , Arthur Weinberg
来源:[J].Fetal & Pediatric Pathology(IF 0.58), 1991, Vol.11 (2), pp.195-210
摘要:We report 5 newborns with a contracted lesser pelvis, imperforate anus (severely stenotic and ectopic anus in 1 case), absent or rudimentary urinary tract, and defective or absent external genitalia, vagina, and uterus but normal gonads. The first 2 patients had small pelvic outl...
作者:Yui Kinjo , Hitoshi Masamoto , Hayase Nitta ...
来源:[J].Case Reports in Obstetrics and Gynecology, 2018, Vol.2018
摘要:... the fetus showed fused lower limbs, bulging abdomen, and absent external genitalia and was diagnosed with type III sirenomelia. On autopsy, no normal bladder was observed, but duodenal atresia, anorectal atresia, and right renal agenesis were found. An intra-abdominal cyst, d...

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