Anorectal malformation associated with klippel–Feil syndrome: A rare association
نویسندگان
چکیده
منابع مشابه
Exstrophy Bladder with Low Anorectal Malformation- A Rare Association
A 4-day-old male newborn, weighing 2.5 Kg, delivered vaginally at 38 weeks presented with malformed external genitalia and a reddish swelling over the lower part of the abdomen and the absent anal opening with a small perineal opening. Pregnancy was uneventful. Maternal serologies for HbsAg, HCV, HIV, Toxoplasma, and Rubella were planned but due to financial reason not done. Physical examinatio...
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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...
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The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by either isolated uterovaginal agenesis or associated with other organ anomalies in genetic women with normal development of secondary sexual characteristics. It affects at least 1 out of 4500 Women. We report an uncommonly seen unique sub type of MRKH syndrome, co-existing with imperforate anus and rectovaginal fistula (RVF) ...
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ژورنال
عنوان ژورنال: Journal of Indian Association of Pediatric Surgeons
سال: 2019
ISSN: 0971-9261
DOI: 10.4103/jiaps.jiaps_161_17