Results 201 to 210 of about 586,789 (263)
Some of the next articles are maybe not open access.
Anorectal malformations associated spinal cord anomalies
Pediatric Surgery International, 2016The present study aims to identify clinical and pathological factors that can predict the risk of spinal cord anomalies (SCA) in patients with anorectal malformations (ARM), the need for neurosurgery, and to define the impact of SCA on the outcome of patients with ARM.A 16-year retrospective analysis of all patients treated at a single tertiary ...
Totonelli G. +7 more
openaire +6 more sources
Congenital anorectal anomalies: MR imaging.
Radiology, 1988Twenty-one patients with anorectal anomalies were evaluated with magnetic resonance (MR) imaging. In seven preoperative patients, MR imaging demonstrated the level of atresia correctly by showing the rectal pouch and sphincter muscles. The exact location and development of the sphincter muscles were estimated and associated anomalies involving the ...
K. C. Pringle +6 more
openaire +4 more sources
Repair of anorectal anomalies in the neonatal period
Pediatric Surgery International, 1990In a 3-year period between 1986 and 1988, 147 patients with anorectal anomalies were seen in our department; 93 were neonates, of which 35 had low malformations treated by anoplasty soon after birth. Fifty-eight had high and intermediate types; 26 of these had defunctioning colostomies.
H. K. Goon
openaire +3 more sources
Surgery of Anorectal Anomalies
Surgical Clinics of North America, 1985This article discusses the disparate views regarding sphincteric anatomy, both normal and abnormal, and describes preoperative procedures for and operative approaches to resolving anorectal anomalies.
Kenneth L. Cox, Pieter A. deVries
openaire +2 more sources
Variations in the Detection of Anorectal Anomalies at Birth among European Cities
European journal of pediatric surgery, 2019Introduction The diagnosis of anorectal malformations (ARMs) is made at birth by perineal examination of the newborn, yet small series reported late diagnosis in almost 13%.
B. Aldeiri +16 more
semanticscholar +1 more source
Congenital familial anorectal anomaly
The American Journal of Surgery, 1973Abstract 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.
E. M. Luttwak +4 more
openaire +3 more sources
Anorectal Anomalies- International Classification
European Journal of Pediatric Surgery, 198280 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.
O. Knutrud +3 more
openaire +3 more sources
Reoperative Surgery for Anorectal Anomalies
Seminars in Pediatric Surgery, 2003Complications 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 +3 more sources
Development and Classification of Anorectal Anomalies
Archives of Surgery, 1964The current classification of congenital anorectal anomalies was established by Partridge and Gough, 1 who divided them into two principal groups: low abnormalities, in which the termination of the bowel is below the pelvic floor (covered anus, ectopic anus, stenosed anus, anal membrane); and high abnormalities, in which the termination of the bowel is
N. McI. Falkiner +2 more
openaire +3 more sources