Seltene Stoffwechselkrankheiten mit rheumatologischer Symptomatik

  • Chapter
Praktische Rheumatologie
  • 4256 Accesses

Zusammenfassung

Angeborene Eisenstoffwechselstörung mit im Laufe der Jahre exzessiv erhöhter Eisenspeicherung in verschiedenen Organen und Gelenken, bedingt durch eine erhöhte intestinale Eisenresorption.

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

Access this chapter

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Chapter
EUR 29.95
Price includes VAT (Germany)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
EUR 149.99
Price includes VAT (Germany)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
EUR 199.99
Price includes VAT (Germany)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free ship** worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Similar content being viewed by others

Literatur

  • Gordon DA (1988) Storage and deposition diseases. Primer on the rheumatic diseases, 10th edn. Arthritis Foundation, Atlanta, pp 225–226

    Google Scholar 

  • Lambert RE, McGuire JL (1997) Iron Storage Diseases. In: Textbook of Rheumatic Diseases, 5th edn, Saunders, Philadelphia, pp 1423–1429

    Google Scholar 

  • Powell LW, Isselbacher KJ (1991) Hemochromatosis. Harrison’s principles of internal medicine, 12th edn. McGraw-Hill, New York, pp 1825–1829

    Google Scholar 

  • Stremmel W (1999) Hämochromatose und Morbus Wilson. Springer, Berlin Heidelberg New York Tokyo, Der Internist 5: 513–521

    Google Scholar 

  • Pietrangelo A (2007) Review Hepatology 46(4): 1291–1301

    Article  CAS  Google Scholar 

Literatur

  • Geminiani G, Olivieri I, Semeria R, Giustarini S, Pasero G (1990) Coexistence of ochronosis and ankylosing spondylitis. J Rheumatol 17: 1707–1709

    Google Scholar 

  • Janocha S, Wolz W, Srsen S, Srsova K, Montagutelli X, Guénet J-L, Grimm T, Kress W, Müller CR (1994) The human gene for alkaptonuria (AKU) maps to chromosome 3 q. Genomics 19: 5

    Article  PubMed  CAS  Google Scholar 

  • Sitaj S (1963) L’arthropathie ochronotique. Alcaptonurie et ochronose. Rheumatologie 15: 93

    CAS  Google Scholar 

  • Skuginna A, Böckmann G (1988) Das Krankheitsbild der Ochronose sowie konservative und operative Therapie. Z Orthop 126: 643–646

    Article  PubMed  CAS  Google Scholar 

  • Stiehl P, Kluger K-M (1994) Gelenkerguß und Befunde bei alkaptonurischer Arthropathie (Ochronose). Z Rheumatol 53: 150–154

    PubMed  CAS  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2012 Springer-Verlag/Wien

About this chapter

Cite this chapter

Peichl, P., Ebner, W. (2012). Seltene Stoffwechselkrankheiten mit rheumatologischer Symptomatik. In: Dunky, A., Graninger, W., Herold, M., Smolen, J., Wanivenhaus, A. (eds) Praktische Rheumatologie. Springer, Vienna. https://doi.org/10.1007/978-3-211-88983-1_7

Download citation

  • DOI: https://doi.org/10.1007/978-3-211-88983-1_7

  • Publisher Name: Springer, Vienna

  • Print ISBN: 978-3-211-88982-4

  • Online ISBN: 978-3-211-88983-1

  • eBook Packages: Medicine (German Language)

Publish with us

Policies and ethics

Navigation