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Archives of Pediatrics & Adolescent Medicine, 1976
A boy, 2 years 5 months of age, was admitted for examination and was found to be mentally retarded. He had a history of low birth weight, covered anus, and perineal fistula. Investigation revealed ventricular septal defect and persistent left superior vena cava, left upper lobe atelectasis, hand and foot anomalies, agenesis or nonfunctioning right ...
Abraham Friedman, Yehezkel Naveh
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A boy, 2 years 5 months of age, was admitted for examination and was found to be mentally retarded. He had a history of low birth weight, covered anus, and perineal fistula. Investigation revealed ventricular septal defect and persistent left superior vena cava, left upper lobe atelectasis, hand and foot anomalies, agenesis or nonfunctioning right ...
Abraham Friedman, Yehezkel Naveh
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Journal of laparoendoscopic & advanced surgical techniques. Part A, 2016
PURPOSE To report our 14 years experience with the laparoscopic-assisted anorectal pull-through (LAARP) for the treatment of male neonates with high imperforate anus.
G. Ruggeri, F. Destro, B. Randi, M. Lima
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PURPOSE To report our 14 years experience with the laparoscopic-assisted anorectal pull-through (LAARP) for the treatment of male neonates with high imperforate anus.
G. Ruggeri, F. Destro, B. Randi, M. Lima
semanticscholar +1 more source
Journal of Pediatric Surgery, 1970
Abstract Another family with occurence of imperforate anus in more than one sibling is added to the literature. Although inperforate anus is rarely a genetically linked anomaly, it may in certain families be inherited in a recessive fashion with a high (25%) risk of appearance of the anomaly in subsequent siblings.
E. David Weinstein, James M. Winkler
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Abstract Another family with occurence of imperforate anus in more than one sibling is added to the literature. Although inperforate anus is rarely a genetically linked anomaly, it may in certain families be inherited in a recessive fashion with a high (25%) risk of appearance of the anomaly in subsequent siblings.
E. David Weinstein, James M. Winkler
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Sonography of imperforate anus.
Radiology, 1983Real-time sonography provides a noninvasive method of determining the level of obstruction in patients with imperforate anus. The authors describe one technique for evaluating this anomaly which was employed in 6 neonates. A pouch-perineum distance of less than 1.5 cm is consistent with a low lesion, while a pouch that terminates above the base of the ...
B A Carroll+2 more
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Esophageal Atresia, Duodenal Atresia, and Imperforate Anus: Triple Atresia
, 2015Triple atresia (TA), that is, esophageal atresia (EA), duodenal atresia (DA), and imperforate anus is very uncommon. We retrospectively analyzed five children who presented with TA from January 2007 to December 2012.
S. Panda+6 more
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Accessory scrotum with imperforate anus
Pediatric Surgery International, 1997Accessory scrotum is the rarest anomaly of the scrotum; less than two dozen cases have been reported. A case of accessory scrotum with imperforate anus is reported.
S. K. Pandit, K. N. Rattan, S. Budhiraja
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Archives of Pediatrics & Adolescent Medicine, 1955
ON JULY 5, 1951, at the local hospital, I delivered spontaneously after a mesiolateral episiotomy on a 22-year-old primipara a living male child whose birth weight was 6 lb. 2 oz. (2780 gm.) Routine inspection of this newborn infant disclosed an imperforate anus. All oral fluids were immediately interdicted.
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ON JULY 5, 1951, at the local hospital, I delivered spontaneously after a mesiolateral episiotomy on a 22-year-old primipara a living male child whose birth weight was 6 lb. 2 oz. (2780 gm.) Routine inspection of this newborn infant disclosed an imperforate anus. All oral fluids were immediately interdicted.
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IMPERFORATE ANUS WITH EXIT THROUGH PROSTATIC URETHRA: REPORT OF THREE CASES
, 1929Congenital anomalies often are of extremely practical as well as of academic interest. I have seen three cases in the past year in which there was no anus, and the child passed feces by way of the urethra.
F. C. Helwig
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Diseases of the Colon & Rectum, 1970
The case report of a 28-year-old man with high imperforate anus and rectourethral fistula (Ladd Type III) is presented. The preoperative findings and operative details are described. The satisfactory result obtained in spite of the patient’s age and the presence of associated vertebral anomalies should encourage attempts at abdominoperineal repair in ...
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The case report of a 28-year-old man with high imperforate anus and rectourethral fistula (Ladd Type III) is presented. The preoperative findings and operative details are described. The satisfactory result obtained in spite of the patient’s age and the presence of associated vertebral anomalies should encourage attempts at abdominoperineal repair in ...
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