Caspian Journal of Pediatrics، جلد ۱، شماره ۱، صفحات ۳۱-۳۴

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عنوان انگلیسی Prenatal diagnosis and postnatal findings of cloacal malformation: a case report
چکیده انگلیسی مقاله 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 fluid-fluid level. Conclusions: The children were followed at regular intervals by an urologist, surgeon and nephrologist throughout life. Medical teams were committed to providing long-term care for children with cloacal anomalies.
کلیدواژه‌های انگلیسی مقاله Cloacal Malformation, Defects, Prenatal Sonographic

نویسندگان مقاله محسن اخوان سپهی | mohsen akhavan sepahi
pediatrics medicine research center, qom university of medical sciences, qom, ir iran.

سازمان اصلی تایید شده: دانشگاه علوم پزشکی قم (Qom university of medical sciences)

زهرا موحدی | zahra movahedi
pediatrics medicine research center


علیرضا ساداتی | alireza sadati
department of pediatrics, hazrat maasomeh hospital


محمدرضا شکراللهی | mohammad reza shokrollahi
pediatrics medicine research center



نشانی اینترنتی http://www.caspianjp.ir/browse.php?a_code=A-10-34-1&slc_lang=en&sid=en
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