[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 nonhemolyticjaundice 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 nonhemolyticjaundice who developed severe unconjugated hyperbilirubinemia shortly after birth and died of kernicterus within months. ... Related articles - All 3 versions
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 nonhemolyticjaundice.6 How ... Related articles - All 3 versions
[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 nonhemolyticjaundice" [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 nonhemolyticjaundice with kernicterus. Pediatrics 1952; 10:169–179. ... Related articles - All 5 versions
沪公网安备号：31010402006960 （网站）31010405000484 （蝌蝌APP）
安全保密
