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Obstruction of the Biliary Limb of the Roux Loop After Successful Kasai Portoenterostomy for Biliary Atresia: Report of Two Cases. [PDF]
Am J Case RepChong CHQ, Lee YY, Mali VP.
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Biliary Atresia with Portal Vein Anomaly: Surgical Challenges and Implications during Kasai Portoenterostomy. [PDF]
J Indian Assoc Pediatr SurgPatil P +5 more
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Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan. [PDF]
Pediatr IntChu CY +7 more
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Prognostic biomarkers of biliary atresia-are we there yet? [PDF]
Pediatr ResVimalesvaran S, Jagadisan B, Dhawan A.
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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
openaire +5 more sources
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
openaire +5 more sources
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 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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2021
Biliary Atresia (BA) affects approximately 1:20,000 babies and is the most frequent cause of surgical jaundice in children. BA presents in the first few weeks of life with pale stools and dark urine in otherwise healthy infants. It is the end result of a destructive inflammatory process of the bile ducts, with unclear origins.
Betalli P., Cheli M., D'Antiga L.
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Biliary Atresia (BA) affects approximately 1:20,000 babies and is the most frequent cause of surgical jaundice in children. BA presents in the first few weeks of life with pale stools and dark urine in otherwise healthy infants. It is the end result of a destructive inflammatory process of the bile ducts, with unclear origins.
Betalli P., Cheli M., D'Antiga L.
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Clinics and Research in Hepatology and Gastroenterology, 2012
Biliary atresia is an obliterative cholangiopathy with progressive hepatobiliary disease, starting from the perinatal period. With a frequency of 1/15-18,000 live births, biliary atresia is the commonest cause of life-threatening liver disease in infants, and fatal if untreated.
Ulrich, Baumann, Benno, Ure
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Biliary atresia is an obliterative cholangiopathy with progressive hepatobiliary disease, starting from the perinatal period. With a frequency of 1/15-18,000 live births, biliary atresia is the commonest cause of life-threatening liver disease in infants, and fatal if untreated.
Ulrich, Baumann, Benno, Ure
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