Zobrazeno 1 - 10
of 38
pro vyhledávání: '"D. C. G. Crabbe"'
Publikováno v:
Pediatric Surgery International. 23:699-702
Lobar emphysema in the neonate is usually congenital, resulting from cartilage deficiency causing bronchomalacia and distal air trapping. Acquired forms are usually associated with chronic lung disease or endobronchial obstruction such as mucus plugg
Autor:
D. C. G. Crabbe, R. J. England
Publikováno v:
Pediatric Surgery International. 22:541-545
The diagnosis of appendicitis in children can be difficult. Misdiagnosis may result in empirical treatment with antibiotics. The aim of this study was to determine whether initial treatment with antibiotics hindered subsequent diagnosis of appendicit
Publikováno v:
Anaesthesia. 53:477-480
Experience with percutaneous dilatational tracheostomy in children is limited. This report discusses two significant complications which occurred following the use of this technique.
Publikováno v:
Hernia. 6:39-41
We report a child who sustained a traumatic hernia of the lower abdominal wall after being thrown forward against the handlebar of his bicycle. This is a rare injury in children, and the clinical features mimic an inguinal haematoma. Suspicion should
Publikováno v:
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie. 17(1)
Roux-en-Y jejunostomy (RYJ) permits enteral feeding in children unable to tolerate oral or intragastric feeds. It avoids many of the complications of nasojejunal and gastrojejunal tubes. Here we report our experience of intubated RYJ. By retrospectiv
Publikováno v:
Journal of Pediatric Surgery. 32:787-789
This report describes separation of thoraco-omphalopagus conjoined twins and management of the hepatobiliary complications that ensued. The livers were fused and, although both infants had gallbladders, the extrahepatic biliary trees were fused. Afte
Autor:
D C G, Crabbe
Publikováno v:
Paediatric respiratory reviews. 4(1)
Congenital isolated tracheo-oesophageal fistula is a rare malformation that presents with a characteristic triad of symptoms: choking and cyanosis on feeding, recurrent lower respiratory tract infection and abdominal distension. Children are invariab
Autor:
Nia Fraser, D. C. G. Crabbe
Publikováno v:
Pediatric surgery international. 18(1)
Gastroschisis is a congenital abdominal-wall defect (AWD) that typically occurs to the right of the umbilicus. Rarely, a mirror variation of the above may occur with a defect to the left of the umbilical cord. This report concerns a neonate born with
Autor:
D. I. Kufeji, D. C. G. Crabbe
Publikováno v:
Pediatric surgery international. 15(1)
Familial inheritance of congenital diaphragmatic hernia is uncommon. We report two siblings with identical bilateral diaphragmatic defects.