Results 291 to 300 of about 111,118 (342)
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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,
F, Cozzi +6 more
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Oesophageal atresia associated with pyloric atresia
The British Journal of Radiology, 1980Pyloroduodenal atresia is a rare and usually isolated anomaly. Crowe and Sumner (1978) recently reported a newborn with pyloroduodenal atresia, isolated oesophageal atresia (Gross Type 1) and cardiac and skeletal malformations. We wish to report a similar case and review the diagnostic techniques that can lead to the correct diagnosis of a second ...
A P, Friedman +3 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 T, Boles, L E, Vassy, M, Ralston
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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 T, Boles, L E, Vassy, M, Ralston
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Seminars in Neonatology, 2003
Biliary atresia (BA) is a congenital obliterative cholangiopathy of unknown aetiology, affecting both the intra- and extrahepatic bile ducts. Although relatively rare, BA must be excluded in any infant with conjugated hyperbilirubinaemia since the prognosis is improved by early diagnosis and prompt surgery.
Hiroyuki, Kobayashi, Mark D, Stringer
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Biliary atresia (BA) is a congenital obliterative cholangiopathy of unknown aetiology, affecting both the intra- and extrahepatic bile ducts. Although relatively rare, BA must be excluded in any infant with conjugated hyperbilirubinaemia since the prognosis is improved by early diagnosis and prompt surgery.
Hiroyuki, Kobayashi, Mark D, Stringer
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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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Seminars in Pediatric Surgery, 2005
Abstract Biliary atresia is a disease characterized by obliteration of both intra- and extrahepatic bile ducts, and presents as conjugated jaundice and pale stools in the first weeks of life. Its aetiology is poorly understood, and many mechanisms have been invoked to explain its pathology.
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Abstract Biliary atresia is a disease characterized by obliteration of both intra- and extrahepatic bile ducts, and presents as conjugated jaundice and pale stools in the first weeks of life. Its aetiology is poorly understood, and many mechanisms have been invoked to explain its pathology.
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Current Opinion in Pediatrics, 1997
Biliary atresia, a progressive obliterative process involving the bile ducts, has its onset in the newborn period. It is characterized by worsening cholestasis, hepatic fibrosis, and cirrhosis, which lead to portal hypertension and a decline in hepatic synthetic function. Untreated, the outcome is uniformly fatal.
W, Middlesworth, R P, Altman
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Biliary atresia, a progressive obliterative process involving the bile ducts, has its onset in the newborn period. It is characterized by worsening cholestasis, hepatic fibrosis, and cirrhosis, which lead to portal hypertension and a decline in hepatic synthetic function. Untreated, the outcome is uniformly fatal.
W, Middlesworth, R P, Altman
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The Lancet, 2009
Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which effective palliative surgery or curative liver transplantation, or both, are available. Good outcomes for infants depend on early referral and timely Kasai portoenterostomy, and thus a high index of suspicion is needed for ...
Jane L, Hartley +2 more
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Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which effective palliative surgery or curative liver transplantation, or both, are available. Good outcomes for infants depend on early referral and timely Kasai portoenterostomy, and thus a high index of suspicion is needed for ...
Jane L, Hartley +2 more
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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.
H S, Asopa, V B, Bhatnagar
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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.
H S, Asopa, V B, Bhatnagar
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Pediatrics In Review, 1989
Biliary atresia is a pathologic entity in which there is obliteration of some portion of the extrahepatic bile ducts. In the past, occlusion of the proximal ducts (at the liver hilus) was referred to as "noncorrectable" (Fig 1). If only the distal duct is occluded (and the proximal duct is patent), the lesion was referred to as "correctable." The ...
E A, Wanek +3 more
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Biliary atresia is a pathologic entity in which there is obliteration of some portion of the extrahepatic bile ducts. In the past, occlusion of the proximal ducts (at the liver hilus) was referred to as "noncorrectable" (Fig 1). If only the distal duct is occluded (and the proximal duct is patent), the lesion was referred to as "correctable." The ...
E A, Wanek +3 more
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