نتایج جستجو برای: high type anorectal malformation

تعداد نتایج: 3188109  

Journal: :Archives of disease in childhood 1983
O H Teixeira K Malhotra J Sellers S Mercer

In 68 patients with anorectal malformations cardiovascular anomalies (CVA) were seen in 15 and genitourinary (GU) anomalies in 30. CVA were more frequent (33%) whenever there was a GU anomaly. Ventricular septal defect was the most frequent lesion. All but 1 CVA occurred with type III anorectal malformation. The complexity of the cardiac lesion did not parallel that of the GU anomaly.

2010
Anand Pandey Ajay N Gangopadhyay Vijayendra Kumar Shiv P Sharma

INTRODUCTION Anorectal malformation, one of the most common congenital defects, may present with a wide spectrum of defects. Almost all male patients present within first few days of life. CASE PRESENTATION A five-month-old baby boy of Indian origin and nationality presented with anal atresia and associated rectourethral prostatic fistula. The anatomy of the malformation and our patient's goo...

Journal: :Journal of Indian Association of Pediatric Surgeons 2017

Journal: :Journal of neonatal surgery 2021

Background: Congenital pouch colon (CPC) is a rare variant of high anorectal malformation. More and more varied associations CPC with other entities are being added to the literature. Case presentation: A 1-day-old male baby presented emergency room marked abdominal distension absent anal opening. On exploration, was found have (Type 2) colonic atresia. This association has not been reported in...

Journal: :iranian journal of pediatric surgery 0
leili mohajerzadeh pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran mohsen rouzrokh pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran ahmad khaleghnejad tabari pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran alireza mirshemirani pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran naser sadeghian pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran javad ghoroubi pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran

purpose : longitudinal follow-up of bowel function in children with anorectal malformations (arms)) as they grow, to determine the anorectal function problems and help to resolve them somedeal. material and methods : this study included 262 patients with arm that operated in our center between 2006 until 2013.patients that definitive reconstruction was performed in another center and underwent ...

Journal: :Prague medical report 2009
P Calda L Haslík Z Zizka M Brestt'ák M Rygl

Intestinal dilatation and hyperechogenic bowel, some typical ultrasonographic features of anorectal malformation, were found in the 21st week of a singleton pregnancy. These findings were associated with unilateral renal agenesis and a single umbilical artery. All prenatally diagnosed anomalies were confirmed postpartum. Development of the sonographic appearance of the anorectal malformation, p...

Journal: :Journal of radiology case reports 2016
Jason K Lee Alexander J Towbin

Currarino syndrome is a congenital disorder, consisting of a triad of anomalies including an anorectal malformation, sacral anomaly, and a presacral mass. Anterior sacral meningoceles are the most common presacral mass. A young child presented to our institution with an unrepaired anorectal malformation and a large anterior sacral meningocele. We describe how the anterior meningocele affected t...

Journal: :iranian journal of pediatric surgery 0
naser sadeghian pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran. sareh pourhassan pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran. nasibeh khaleghnejad tabari pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran. anahita sadeghian pediatric surgery research center, shahid beheshti university of medical sciences, tehran, iran.

introduction: rectal prolapse refers to extrusion of mucosa or the full thickness wall of the rectum through the anal sphincter, which is more common between infancy and 4 years of age and has a high incidence in the first year of life. it is considered as a sign of an underlying clinical condition causing an increased intra‑abdominal pressure, pelvic floor weakness or poor root innervations as...

2017
Prince Raj Hirendra Birua

Congenital pouch colon (CPC) or short colon syndrome is a rare type of anorectal malformation(ARM). Type V is the rarest form of CPC. We present a 1-day-old male child with type V CPC with prune belly syndrome and congenital anterior urethrocutaneous fistula (CAUF).

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