نتایج جستجو برای: pyloric atresia

تعداد نتایج: 13584  

2014
Yogender Singh Kadian KN Rattan

The mainstay of diagnosis of congenital pyloric atresia is by plain X-ray of the abdomen showing a large gas bubble with no gas distally. But very rarely it can be associated with distal duodenal atresia when the baby may present as lump abdomen. In such a situation apart from the X-ray, another radiological investigation is needed to delineate the exact nature of the lump. Since the role of ul...

2013
Sushmita Bhatnagar

Successful management of a neonate with type II pyloric atresia is reported and the relevant literature has been briefly reviewed.

2012
Yousuf Aziz Khan Naima Zamir

Congenital pyloric atresia is a rare anomaly accounting for less than 1% of upper GI atresias. It may occur in isolation or in association with other congenital anomalies, epidermolysis bullosa being the most frequent. It presents with upper abdominal distension, non-bilious vomiting or rarely with complications as aspiration pneumonia, electrolyte imbalance or gastric perforation. Though iatro...

2016
Manoj Saha

Anorectal malformation (ARM) is one of the most common congenital anomaly that requires emergency surgery in the neonatal period. ARMs are frequently associated with other life threatening congenital anomalies. Commonly associated anomalies are genito-urinary, cardiovascular, gastro-intestinal, skeletal and spinal. Alimentary tract anomalies are frequently masked by the intestinal obstruction p...

Journal: :La Pediatria medica e chirurgica : Medical and surgical pediatrics 2012
L Costa S F Chiarenza S D'Agostino L Musi

The first cases of atresia or web in the pyloric and prepyloric regions were described in the literature since 1937. To date, only one case of atresia at the junction between the fundus and the body of the stomach has been reported. We want to describe a complex case with incomplete atresia between fundus and gastric body, with left lateral diaphragmatic hernia, treated in several stages by end...

Journal: :Journal of Case Reports 2016

Journal: :Journal of Pediatric Surgery Case Reports 2014

Journal: :Bangladesh Journal of Child Health 1970

2010
Ken Natsuga Wataru Nishie Satoru Shinkuma Ken Arita Hideki Nakamura Makiko Ohyama Hitoshi Osaka Takeshi Kambara Yoshiaki Hirako Hiroshi Shimizu

Plectin is a cytoskeletal linker protein which has a long central rod and N- and C-terminal globular domains. Mutations in the gene encoding plectin (PLEC) cause two distinct autosomal recessive subtypes of epidermolysis bullosa: EB simplex (EBS) with muscular dystrophy (EBS-MD), and EBS with pyloric atresia (EBS-PA). Previous studies have demonstrated that loss of full-length plectin with resi...

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