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[PDF] from banglajol.infoM Haque - Journal of Medicine, 2011 - banglajol.info
... 87 Page 3. Conclusion: Crigler-Najjar syndrome type 2 is an extremely rare, congenital
non-hemolytic unconjugated hyperbilirubinemia caused by deficiency of UDP-
glucuronosyltransferase. ... Congenital familial nonhemolytic jaundice with kernicterus. ...
Related articles - All 2 versions
MG Bartlett… - Seminars in Perinatology, 2011 - Elsevier
... 72. Crigler–Najjar Syndrome Types I and II. In 1952, Crigler and Najjar described 7 infants
with congenital familial nonhemolytic jaundice who developed severe unconjugated
hyperbilirubinemia shortly after birth and died of kernicterus within months. ...
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L Rosti, L Lambertini, I Stucchi… - Pediatrics, 2011 - Am Acad Pediatrics
... infants with he- molytic disease caused by Rhesus/AB0 incompatibility, the association of neo-
natal jaundice with autism and/or schizophrenia was unclear, although in these situations bilirubin
may cross the blood-brain barrier more easily than in nonhemolytic jaundice.6 How ...
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[PDF] from puc.clN Roy-Chowdhury, X Wang, J Roy-Chowdhury… - 2011 - cursos.puc.cl
... GILBERT'S SYNDROME — The most common inherited disorder of bilirubin glucuronidation
is Gilbert's syndrome, which has also been called "constitutional hepatic dysfunction" and "familial
nonhemolytic jaundice" [2]. Although many patients present as isolated cases, the ...
Cited by 2 - Related articles - View as HTML
Y Maruo, F Ozgenc, Y Mimura, Y Ota… - Journal of pediatric …, 2011 - journals.lww.com
... In: Braunwald E, Fauci AS, Kasper DL, et al, eds. Principles of Internal Medicine. 15th ed. New
York: McGraw-Hill; 2001:1715–20. Cited Here... 2. Crigler JF, Najjar VA. Congenital familial
nonhemolytic jaundice with kernicterus. Pediatrics 1952; 10:169–179. ...
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