01 March 2001
Diagnostic problems of with determination of the cause of hyperbilirubinemia in a child with Gilbert's syndrome and deficiency of alpha-1-antitrypsin
Dariusz Marek Lebensztejn , Maria E. Sobaniec-Łotowska , Maciej Kaczmarski , Jolanta Tobolczyk , Justyna ChwiećkoCase Rep Clin Pract Rev 2001; 2(1):65-69 :: ID: 474656
Abstract
The authors present diagnostic problems with determination of the reasons for persistent hyperbilirubinemia accompanied by histopathologic characteristics of liver damage in a 12-year-old girl, caused by congenital alpha-1-antitrypsin deficiency and Gilbert's syndrome.
Keywords: free hyperbilirubinemia, Gilbert's syndrome, congenital alpha-1-antitrypsin deficiency
734
In Press
Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.953543
Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.954216
Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.954932
Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.954146
Most Viewed Current Articles
07 Dec 2021 : Case report
28,712,695
DOI :10.12659/AJCR.934347
Am J Case Rep 2021; 22:e934347
06 Dec 2021 : Case report 
180,721
DOI :10.12659/AJCR.934406
Am J Case Rep 2021; 22:e934406
21 Jun 2024 : Case report
124,419
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
08 May 2026 : Case report
95,462
DOI :10.12659/AJCR.952158
Am J Case Rep 2026; 27:e952158