Literature DB >> 9236515

Gilbert's syndrome co-existing with and masking hereditary spherocytosis.

S Sharma1, S J Vukelja, S Kadakia.   

Abstract

An unusual case of co-existing Gilbert's syndrome and hereditary spherocytosis is reported. Diagnostic strategies are presented, and the literature is reviewed for simultaneous presence of these disorders.

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Mesh：

Year:  1997        PMID： 9236515     DOI： 10.1007/s002770050302

Source DB:  PubMed          Journal:  Ann Hematol        ISSN： 0939-5555            Impact factor:   3.673


  5 in total

1.  Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.

Authors:  Shigeo Iijima; Takehiko Ohzeki; Yoshihiro Maruo
Journal:  Yonsei Med J       Date:  2011-03       Impact factor: 2.759

2.  Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

Authors:  Jae Hee Lee; Kyung Rye Moon
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2014-12-31

3.  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

4.  Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.

Authors:  Joo Hyung Han; Seung Kim; Hoon Jang; So Won Kim; Min Goo Lee; Hong Koh; Ji Hyun Lee
Journal:  PLoS One       Date:  2015-06-24       Impact factor: 3.240

5.  Acoustophoretic Orientation of Red Blood Cells for Diagnosis of Red Cell Health and Pathology.

Authors:  Laura G Rico; Jordi Juncà; Mike D Ward; Jolene A Bradford; Jorge Bardina; Jordi Petriz
Journal:  Sci Rep       Date:  2018-10-24       Impact factor: 4.379
  5 in total

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