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   Prenatal Diagnosis and Postnatal Findings of Cloacal Malformation: A Case Report  
   
نویسنده Akhavan Sepahi Mohsen ,Movahedi Zahra ,Sadati Alireza ,Shokrollahi Mohammad Reza
منبع Caspian Journal Of Pediatrics - 2015 - دوره : 1 - شماره : 1 - صفحه:31 -34
چکیده    Introduction: cloacal malformation is an extremely rare fetal pathological condition but an important anomaly that presents as a variety of defects. it predominantly affects females, with prevalence of 1 in 50,000 births. prenatal ultrasonography usually showed oligohydramnios and the fetus having a large cystic mass in the lower abdomen with a single septum, bilateral hydronephrosis, ambiguous genitalia and a single umbilical artery. postnatal finding including ambiguous genitalia and rectal atresia with a single perineal opening. case report: the purpose of this case series was to illustrate characteristic prenatal sonographic features of cloacal malformation by using imaging from 3 cases seen in all academic centers to augment published data. the imaging feature common to all cases was a central cystic pelvic mass containing a characteristic fluidfluid level. conclusions: the children were followed at regular intervals by an urologist, surgeon and nephrologist throughout life. medical teams were committed to providing longterm care for children with cloacal anomalies.
کلیدواژه Cloacal Malformation ,Defects ,Prenatal Sonographic
آدرس Qom University Of Medical Sciences And Health Services, Pediatrics Medicine Research Center, ایران, Qom University Of Medical Sciences And Health Services, Pediatrics Medicine Research Center, ایران, Qom University Of Medical Sciences And Health Services, Hazrat Maasomeh Hospital, Department Of Pediatrics, ایران, Qom University Of Medical Sciences And Health Services, Pediatrics Medicine Research Center, ایران
 
     
   
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