Oslo Syndrome - The iron brother of Wilson's disease. - E-book - ePub

Edition en anglais

Adrian Tudor

,

Seideman David

,

Lucas Smith

,

Jacob Adams

,

Diamandis Carolina

Note moyenne 
Evidence-based medicine has shown for many years that homozygous mutations of the HFE gene H63D are by no means negligible. Not only can it provoke, usually... Lire la suite
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Résumé

Evidence-based medicine has shown for many years that homozygous mutations of the HFE gene H63D are by no means negligible. Not only can it provoke, usually after a second hit, rather mild classical hemochromatosis, but it can also cause numerous other disorders of iron metabolism, such as Oslo-Syndrome. The latter is a severe disease which leads to multiple organ damages and is - for reasons that remain in the dark - not as known as Wilson's disease which is a very similar syndrome caused by copper.

Caractéristiques

  • Date de parution
    23/05/2022
  • Editeur
  • ISBN
    978-3-7562-1927-8
  • EAN
    9783756219278
  • Format
    ePub
  • Nb. de pages
    37 pages
  • Caractéristiques du format ePub
    • Pages
      37
    • Taille
      1 569 Ko
    • Protection num.
      pas de protection

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À propos des auteurs

Clinician, specialized in family and community medicine. Professor of the scientific study of consciousness with the Jewish University of Colorado (JUC) and clinician in a practice for patients with rare diseases. Clinician, internist and endocrinologist. Senior doctor in an outpatient clinic for rare diseases. Neurologist, neuroimmunologist, former member of the International H63D Syndrome Research Consortium. Clinician and General Director of LCG Research Greece and of the Lazar Medical Consortium Group. Former chief resident with hospitals in eastern Europe, now clinician and researcher with LCG Research.

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