Literature DB >> 23780771

Severe unconjugated hyperbilirubinaemia: one and one makes three?

Kushal Naha1, Sowjanya Dasari, G Vivek, Manjunath Hande, Vasudev Acharya.   

Abstract

A 38-year-old housewife presented with a 3-month history of gradually progressive fatigue and deepening jaundice as well as a history of mild fluctuating jaundice since childhood. General examination revealed an obvious icterus. Systemic examination was normal. Laboratory tests confirmed unconjugated hyperbilirubinaemia. Further evaluation yielded a diagnosis of vitamin B12 deficiency on a background of Gilbert's syndrome.

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Year:  2013        PMID： 23780771      PMCID： PMC3703004          DOI： 10.1136/bcr-2013-009962

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN： 1757-790X


  10 in total

1.  Concomitant Gilbert's syndrome and thalassemia trait.

Authors:  G Singh; M P Agarwal
Journal:  J Assoc Physicians India       Date:  2003-03

2.  Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

Authors:  Dipti Kumar; Ankit Parakh; Sunita Sharma
Journal:  J Pediatr Hematol Oncol       Date:  2012-01       Impact factor: 1.289

Review 3.  Megaloblastic anemia and other causes of macrocytosis.

Authors:  Florence Aslinia; Joseph J Mazza; Steven H Yale
Journal:  Clin Med Res       Date:  2006-09

4.  Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome.

Authors:  Kenichi Sugita; Yoshihiro Maruo; Hidemitsu Kurosawa; Akira Tsuchioka; Toshio Fujiwara; Asami Mori; Hiroshi Ideguchi; Mitsuoki Eguchi
Journal:  Pediatr Int       Date:  2007-08       Impact factor: 1.524

5.  The reciprocal relation between caloric intake and the degree of hyperbilirubinemia in Gilbert's syndrome.

Authors:  B F Felsher; D Rickard; A G Redeker
Journal:  N Engl J Med       Date:  1970-07-23       Impact factor: 91.245

6.  Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects.

Authors:  J Borlak; T Thum; O Landt; K Erb; R Hermann
Journal:  Hepatology       Date:  2000-10       Impact factor: 17.425

7.  Hereditary spherocytosis coexisting with Gilbert's syndrome: a diagnostic dilemma.

Authors:  P K Garg; A Kumar; N Teckchandani; N S Hadke
Journal:  Singapore Med J       Date:  2008-11       Impact factor: 1.858

8.  An unusual cause for recurrent jaundice in an otherwise healthy male.

Authors:  Sowjanya Dasari; Kushal Naha; Mukhyaprana Prabhu
Journal:  Australas Med J       Date:  2012-10-31

9.  Severe jaundice in a patient with a previously undescribed glucose-6-phosphate dehydrogenase (G6PD) mutation and Gilbert syndrome.

Authors:  Ernest Beutler; Terri Gelbart; William Miller
Journal:  Blood Cells Mol Dis       Date:  2002 Mar-Apr       Impact factor: 3.039

10.  A case of concomitant Gilbert's syndrome and hereditary spherocytosis.

Authors:  Hee Jung Lee; Hee Seok Moon; Eaum Seok Lee; Seok Hyun Kim; Jae Kyu Sung; Byung Seok Lee; Hyun Yong Jeong; Heon Young Lee; Young Jae Eu
Journal:  Korean J Hepatol       Date:  2010-09
  10 in total
  1 in total

1.  Occurrence of Recurrent Aphthous Stomatitis (RAS) as a Rare Oral Manifestation in a Patient with Gilbert's Syndrome.

Authors:  Artak Heboyan; Anna Avetisyan; Hans Erling Skallevold; Dinesh Rokaya; Vinay Marla; Anna Vardanyan
Journal:  Case Rep Dent       Date:  2021-04-16
  1 in total

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