Results 161 to 170 of about 4,190 (206)
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FAMILIAL ANORECTAL ANOMALIES

Pediatrics, 1961
A family is reported in which all four children, equally divided between the sexes, manifested anorectal anomalies ranging from an anorectal stenosis to a type III imperforate anus. There is no knowledge of similar anomalies in other relatives. It is suggested that in this family the anomaly could be caused by either an autosomal dominant or recessive ...
D W, VANGELDER, H W, KLOEPFER
openaire   +2 more sources

Congenital familial anorectal anomaly

The American Journal of Surgery, 1973
Abstract A man born with severe anal stenosis and his two sons, each with imperforate anus, are described. The occurrence of the malformation in father and both sons indicates for the first time a possible dominant autosomal inheritance.
J, Manny   +4 more
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Anorectal Anomalies- International Classification

European Journal of Pediatric Surgery, 1982
80 patients with anorectal anomalies were admitted to the Paediatric Surgical Service of the National Hospital of Norway during the five year period 1970--74. The anomalies were classified according to the International Classification which was found to be of obvious value in comparing material and results.
A, Paus   +3 more
openaire   +2 more sources

Surgery of Anorectal Anomalies

Surgical Clinics of North America, 1985
This article discusses the disparate views regarding sphincteric anatomy, both normal and abnormal, and describes preoperative procedures for and operative approaches to resolving anorectal anomalies.
P A, deVries, K L, Cox
openaire   +2 more sources

Associated anomalies in cases with anorectal anomalies

American Journal of Medical Genetics Part A, 2018
Anorectal anomalies (ARA) are common congenital anomalies. The etiology of ARA is unclear and its pathogenesis is controversial. Cases with ARA often have other non‐ARA‐associated congenital anomalies. The purpose of this study was to assess the prevalence and the types of these associated anomalies in a defined population.
Claude Stoll   +3 more
openaire   +2 more sources

Reoperative Surgery for Anorectal Anomalies

Seminars in Pediatric Surgery, 2003
Complications occur during the repair of anorectal malformations relatively frequently. Unfortunately, these complications are often preventable. Furthermore, the consequences of these complications are significant. Not only do patients experience unnecessary pain and suffering, but a secondary operation always renders less optimal functional results ...
Alberto, Peña   +3 more
openaire   +2 more sources

Anorectal anomaly in Pfeiffer syndrome

Clinical Dysmorphology, 1993
A Japanese girl with Pfeiffer syndrome is described. She has clinical and radiological manifestations typical of the syndrome. In addition, she had an imperforate anus not described previously in the syndrome. This seems to expand the phenotype associated with Pfeiffer syndrome or represent a new acrocephalosyndactyly syndrome.
H, Ohashi   +6 more
openaire   +2 more sources

Total anorectal reconstruction following congenital anorectal anomaly

Diseases of the Colon & Rectum, 1976
Following several unsuccessful postnatal attempts at anoplasty to correct anal atresia with a rectovaginal fistula, the patient, 20 years later, underwent an anorectal sphincteric construction using a gracilis-muscle transplant. The five-stage procedure, which extended over a period of two years, resulted in highly satisfactory continence and full ...
E T, Jacob   +3 more
openaire   +2 more sources

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