Anorectal Malformation with Associated Duodenal Obstruction and Uterus Didelphys
نویسندگان
چکیده
منابع مشابه
Late Presentation of a Congenital Intrinsic Duodenal Obstruction in a Patient with Anorectal Malformation
Anorectal Malformations are known to be associated with various other congenital anomalies including duodenal atresia. An association of congenital intrinsic duodenal obstruction causing partial duodenal obstruction in a patient with anorectal malformation is not described in literature. We describe a case of delayed presentation of congenital intrinsic duodenal obstruction in a child with high...
متن کاملUrogenital anomalies associated with anorectal malformation
Background: The objective of the paper is to review the incidence and types of associated urogenital anomalies (U.G.A.) we encountered in patients with anorectal malformations (A.R.M.) and compare the results with previously published world literature. Materials and Methods: Retrospective review was done of 220 cases of A.R.M., treated from May 2002 to April 2003. All patients routinely underwe...
متن کاملAnorectal malformation: familial aspects and associated anomalies.
One hundred and sixty nine patients with anorectal malformation were studied: there were 108 boys, 60 girls, and one case of intersex. Low malformations were more common in both sexes. Over half the subjects had associated malformations. These were more common in the group with high malformations. There was no difference between the sexes in this respect. A family history of similar malformatio...
متن کاملAnnular pancreas associated with duodenal obstruction.
DESCRIPTION A preterm neonate weighing 1360 g was born at 33+2 weeks’ gestation with severe polyhydramnios. She was transferred, directly after delivery, to our neonatal intensive care unit presenting with distended upper abdomen and vomiting. A plain film of the abdomen (figure 1) was performed with the suspicion of duodenal atresia and showed a markedly distended stomach (S) and proximal duod...
متن کاملIdentical twins with uterus didelphys and duplex kidneys.
Congenital uterine abnormalities occur as a result of partial or complete failure of Mullerian duct fusion probably about the fifth or sixth week of fetal life. Maternal and/or placental factors have been implicated. There are a few reports of a double uterus occurring in sisters and their mothers (Polishuk & Ron, 1974; Prucha, 1983) which suggest a dominant autosomal gene as a possible genetic...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: West Indian Medical Journal
سال: 2016
ISSN: 0043-3144
DOI: 10.7727/wimj.2015.557