Oslo Syndrome

Zusatztext

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.

Autorenportrait

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

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