Interní Med. 2017; 19(1): 39-41 | DOI: 10.36290/int.2017.007

Genetic hemochromatosis, one cause, more illnesses

MUDr. Bedřich Staňka1, MUDr. Mgr. Jaroslav Maceček, Ph.D.1, MUDr. Petr Konvička2
1Gastroenterologické oddělení Nemocnice Prostějov, Středomoravská Nemocniční a. s., člen skupiny AGEL, 2Interní oddělení Nemocnice Přerov, Středomoravská Nemocniční a. s., člen skupiny AGEL

The case study describes a hospitalized patient with seemingly unequivocal diagnosis of diabetes mellitus. Based on the examination,

however, an increased amount of various non-specific symptoms, which in turn was completed with a diagnosis, which is

generally little thought, therefore genetic hemochromatosis and this case indicates the necessity of complex differential diagnosis.

The patient was successfully treated by repeated venipuncture.

Keywords: genetic hemochromatosis, iron metabolism, HFE gene

Published: February 1, 2017  Show citation

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Staňka B, Maceček J, Konvička P. Genetic hemochromatosis, one cause, more illnesses. Interní Med. 2017;19(1):39-41. doi: 10.36290/int.2017.007.
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References

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  2. Lanktree MB, Sadikovic B, Waye JS, et al. Clinical evaluation of a hemochromatosis next-generation sequencing gene panel. Eur J Haematol. 2016. Go to original source... Go to PubMed...
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