Skip to main content
Log in

A rare combination of two inherited disorders in one patient: pyruvate kinase deficiency and hemochromatosis

  • Letter to the Editor
  • Published:
Annals of Hematology Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Valentine WN, Tanaka KR, Miwa S (1961) A specific erythrocyte glycolytic enzyme defect (pyruvate kinase) in three subjects with congenital non-spherocytic hemolytic anemia. Trans Assoc Am Physicians 74:100–110

    PubMed  CAS  Google Scholar 

  2. Blume KG, Busch D, Arnold H, Löhr GW (1971) Klinische Untersuchungen zur hereditären nichtsphärozytären hämolytischen Anämie bei Pyruvatkinasemangel der Erthrozyten. Klin Wschr 49:228–230. doi:10.1007/BF01495990

    Article  PubMed  CAS  Google Scholar 

  3. Blume KG, Löhr GW, Praetsch O, Rüdiger HW (1968) Beitrag zur Populationsgenetik der Pyruvatkinase menschlicher Erythrozyten. Humangenetik 6:261–265. doi:10.1007/BF00291870

    Article  PubMed  CAS  Google Scholar 

  4. Merryweather-Clarke AT, Pointon JJ, Sherman JD, Robson KJH (1997) Global prevalence of putative haemochromatosis mutations. J Med Genet 34:275. doi:10.1136/jmg.34.4.275

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Karl G. Blume.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Arnold, H., Blume, K.G. A rare combination of two inherited disorders in one patient: pyruvate kinase deficiency and hemochromatosis. Ann Hematol 88, 815–816 (2009). https://doi.org/10.1007/s00277-008-0681-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00277-008-0681-7

Keywords

Navigation