Literature DB >> 15581751

Congenital spherocytosis with hereditary hemochromatosis without pathogenic mutations in the HFE gene.

Malika Ichiche1, Patrick Lacor, Anita Hoorens, Jan Vanden Brande, Hanny Brussaard, Danny Vanstraelen.   

Abstract

We report a case of an 80-year-old woman with congenital spherocytosis who presented with massive iron overload. Iatrogenic iron overload could be ruled out. Familial history was suggestive of hereditary hemochromatosis; however, molecular genetic testing for the most common HFE mutations remained negative. The patient was treated successfully with phlebotomies. The hypothesis that this patient suffered from hereditary hemochromatosis is discussed on the basis of a brief review of the literature.

Entities:  

Year:  2004        PMID: 15581751     DOI: 10.1016/j.ejim.2004.06.013

Source DB:  PubMed          Journal:  Eur J Intern Med        ISSN: 0953-6205            Impact factor:   4.487


  3 in total

1.  Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing.

Authors:  Li Qin; Yanbo Nie; Hong Zhang; Long Chen; Donglei Zhang; Yani Lin; Kun Ru
Journal:  J Hum Genet       Date:  2020-01-24       Impact factor: 3.172

2.  Hereditary xerocytosis revisited.

Authors:  Natasha M Archer; Boris E Shmukler; Immacolata Andolfo; David H Vandorpe; Radhakrishnan Gnanasambandam; John M Higgins; Alicia Rivera; Mark D Fleming; Frederick Sachs; Philip A Gottlieb; Achille Iolascon; Carlo Brugnara; Seth L Alper; David G Nathan
Journal:  Am J Hematol       Date:  2014-07-21       Impact factor: 10.047

3.  Coinheritance of hereditary spherocytosis and reversibility of cirrhosis in a young female patient with hereditary hemochromatosis.

Authors:  A Höblinger; C Erdmann; C P Strassburg; T Sauerbruch; F Lammert
Journal:  Eur J Med Res       Date:  2009-04-16       Impact factor: 2.175

  3 in total

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