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作者:Rita A. Mukhtar , Laurence S. Baskin , Peter G. Stock ...
来源:[J].Journal of Pediatric Surgery(IF 1.383), 2009, Vol.44 (12), pp.e31-e33Elsevier
摘要:Abstract(#br)Cloacal dysgenesis sequence (CDS) is a severe hindgut malformation occurring in 1:50,000 to 250,000 live births (Qureshi et al. Prenatal diagnosis of cloacal dysgenesis sequence: differential diagnosis from other forms of fetal obstructive uropathy. Fetal Diagn Ther ...
作者:Selen Gursoy Erzincan , N. Cenk Sayin , Cihan Inan ...
来源:[J].Journal of Obstetrics and Gynaecology Research(IF 0.841), 2020, Vol.46 (3), pp.527-530Wiley
摘要:Abstract(#br)Cloacal dysgenesis sequence occurs as a result of complete developmental failure of the urorectal septum. Typically, the sequence is featured by a smooth perineum, without any urethral, genital or anal openings. Its clinical manifestation differs throughout gestation...
作者:Archana Bargaje , John F. Yerger , Adib Khouzami ...
来源:[J].Annals of Diagnostic Pathology(IF 0.975), 2006, Vol.12 (1), pp.62-66Elsevier
摘要:Abstract(#br)Cloacal dysgenesis sequence is a rare congenital malformation seen in 1:50 000 to 250 000 neonates. It shows a phallus-like structure, smooth perineum, and absence of urethral, vaginal, and anal openings as primary malformations. We report a case of a 4-day-old prete...
作者:Xiayuan Liang , Olga B. Ioffe, , Chen-Chih J. Sun
来源:[J].Pediatric and Developmental Pathology(IF 0.859), 1998, Vol.1 (4), pp.281-288Springer
摘要:ABSTRACT(#br) Cloacal dysgenesis is a rare malformation sequence. We studied cloacal dysgenesis in four fetuses, including three at 18–22 weeks of gestation. All four fetuses showed a smooth perineum with absence of anal, urethral, and/or vaginal openings. The urinary bladde...
作者:Bargaje Archana , Yerger John F , Khouzami Adib ...
来源:[J].Annals of diagnostic pathology(IF 0.975), 2008, Vol.12 (1), pp.62-6PubMed
摘要:Cloacal dysgenesis sequence is a rare congenital malformation seen in 1:50000 to 250000 neonates. It shows a phallus-like structure, smooth perineum, and absence of urethral, vaginal, and anal openings as primary malformations. We report a case of a 4-day-old preterm female neona...
作者:Sahinoglu Zeki , Mulayim Baris , Ozden Selcuk ...
来源:[J].Prenatal diagnosis(IF 2.683), 2004, Vol.24 (1), pp.10-6PubMed
摘要:OBJECTIVE(#br)Cloacal dysgenesis sequence is a lethal malformation, which usually requires termination. In this study, our aim was to evaluate the prenatal and postnatal diagnostic features of cloacal dysgenesis sequence and review the management of the patients.(#br)MATERIAL AND...
作者:Ramaswamy Rajendran Baz Rayan Ahmed Alchami Marwan Mukattash Ghazi pediatric surgery
来源:[J].Pediatric Urology Case Reports, 2019, Vol.6 (4)小儿泌尿外科病例报告
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:Qureshi F , Jacques S M , Yaron Y ...
来源:[J].Fetal diagnosis and therapy(IF 1.902), 1998, Vol.13 (2), pp.69-74PubMed
摘要:Cloacal dysgenesis sequence (CDS) is a rare cause of fetal obstructive uropathy (FOU). The prenatal differentiation of CDS from other FOU is important because CDS is not amenable to in utero surgical intervention in the form of vesicoamniotic shunts. We evaluated the prenatal cha...
作者:Liang X , Ioffe O B , Sun C C
来源:[J].Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society(IF 0.859), 1998, Vol.1 (4), pp.281-8PubMed
摘要:Cloacal dysgenesis is a rare malformation sequence. We studied cloacal dysgenesis in four fetuses, including three at 18-22 weeks of gestation. All four fetuses showed a smooth perineum with absence of anal, urethral, and/or vaginal openings. The urinary bladder was dilated in 3 ...

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