Results 301 to 310 of about 115,582 (346)
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Esophageal atresia, choanal atresia, and dysautonomia
Journal of Pediatric Surgery, 1991Patients with esophageal atresia (EA) or choanal atresia (CA) manifest similar clinical and pathophysiological features. To determine the significance of this observation, the clinical records of 80 patients with EA and 57 with CA were reviewed. This survey showed that similarities between the two conditions included inspiratory and expiratory dyspnea,
G. Fiocca +13 more
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Journal of Pediatric Surgery, 1976
Eleven infants with colon atresia have been managed by staged procedure with survival and good health in ten. Complications have been relatively few. At the initial operation the proximal atretic segment is exteriorized as an end colostomy. Such a procedure is simple and safe, results in rapid relief of the obstruction, and permits normal feeding by ...
E. Thomas Boles +2 more
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Eleven infants with colon atresia have been managed by staged procedure with survival and good health in ten. Complications have been relatively few. At the initial operation the proximal atretic segment is exteriorized as an end colostomy. Such a procedure is simple and safe, results in rapid relief of the obstruction, and permits normal feeding by ...
E. Thomas Boles +2 more
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Pediatrics In Review, 2022
Intestinal atresia is a form of congenital bowel obstruction that requires operative repair in the early neonatal period. Duodenal atresia and jejunoileal (JI) atresia are appropriately seen as distinct entities. Both can be suspected with fetal imaging, which can assist with prenatal counseling of families. Duodenal atresia is more commonly associated
Barrie S, Rich +2 more
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Intestinal atresia is a form of congenital bowel obstruction that requires operative repair in the early neonatal period. Duodenal atresia and jejunoileal (JI) atresia are appropriately seen as distinct entities. Both can be suspected with fetal imaging, which can assist with prenatal counseling of families. Duodenal atresia is more commonly associated
Barrie S, Rich +2 more
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Seminars in Pediatric Surgery, 2005
Biliary atresia (BA) remains a devastating disease of infants. It is still a disease of largely unknown etiology although many hypotheses such as an aberrant early bile duct development, perinatal viral infection, aberrant immune response, and abnormalities of bile acids have all been suggested as possibly etiologically important.
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Biliary atresia (BA) remains a devastating disease of infants. It is still a disease of largely unknown etiology although many hypotheses such as an aberrant early bile duct development, perinatal viral infection, aberrant immune response, and abnormalities of bile acids have all been suggested as possibly etiologically important.
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Journal of Pediatric Surgery, 2005
Colonic atresia (CA) is one of the rarest causes of neonatal intestinal obstructions, and no large series can be reported. Therefore, we did perform a retrospective clinical trial to delineate our CA cases and carry out a literature survey.We reviewed the charts of CA cases treated in our center between 1992 and 2002.
Barlas Etensel +6 more
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Colonic atresia (CA) is one of the rarest causes of neonatal intestinal obstructions, and no large series can be reported. Therefore, we did perform a retrospective clinical trial to delineate our CA cases and carry out a literature survey.We reviewed the charts of CA cases treated in our center between 1992 and 2002.
Barlas Etensel +6 more
openaire +3 more sources
Baillière's Clinical Gastroenterology, 1989
Biliary atresia remains a serious and devastating surgical condition of early childhood. Despite portoenterostomy almost half of these children remain jaundiced and suffer repeated attacks of bacterial cholangitis or variceal haemorrhage. Recently liver transplantation offers fresh hope for these children.
K C, Tan, E R, Howard
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Biliary atresia remains a serious and devastating surgical condition of early childhood. Despite portoenterostomy almost half of these children remain jaundiced and suffer repeated attacks of bacterial cholangitis or variceal haemorrhage. Recently liver transplantation offers fresh hope for these children.
K C, Tan, E R, Howard
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Journal of Pediatric Surgery, 1998
A 4-day-old black male underwent laparotomy for intestinal obstruction. At surgery, multiple jejunal atresias (type IV) of the jejunum were detected. As an incidental finding, atresia of the appendix was also present. The jejunal atresia was repaired, and resection of the tip of the cecal pole and atretic appendix was performed.
Soraya Verhaart +2 more
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A 4-day-old black male underwent laparotomy for intestinal obstruction. At surgery, multiple jejunal atresias (type IV) of the jejunum were detected. As an incidental finding, atresia of the appendix was also present. The jejunal atresia was repaired, and resection of the tip of the cecal pole and atretic appendix was performed.
Soraya Verhaart +2 more
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Current Opinion in Gastroenterology, 2019
Purpose of review Biliary atresia is a poorly understood deadly disease. Genetic predisposition factors are suspected albeit not firmly established. This review summarizes recent evidence of genetic alterations in biliary atresia.
M. Girard, G. Panasyuk
semanticscholar +1 more source
Purpose of review Biliary atresia is a poorly understood deadly disease. Genetic predisposition factors are suspected albeit not firmly established. This review summarizes recent evidence of genetic alterations in biliary atresia.
M. Girard, G. Panasyuk
semanticscholar +1 more source
Current Treatment Options in Cardiovascular Medicine, 2000
Untreated, the prognosis for patients with tricuspid atresia (TA) is poor. Recent advances in medical and surgical therapy, particularly the application of Fontan principle, have markedly improved the long-term outlook for children with this condition.
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Untreated, the prognosis for patients with tricuspid atresia (TA) is poor. Recent advances in medical and surgical therapy, particularly the application of Fontan principle, have markedly improved the long-term outlook for children with this condition.
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The Indian Journal of Pediatrics, 1970
A case of duodenal atresia is presented in a child of 1 1/2 years. Duodeno-jejunostomy was done and the patient recovered.
V. B. Bhatnagar, H. S. Asopa
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A case of duodenal atresia is presented in a child of 1 1/2 years. Duodeno-jejunostomy was done and the patient recovered.
V. B. Bhatnagar, H. S. Asopa
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