Oslo Syndrome

The iron brother of Wilson's disease.

Adrian Tudor, Seideman David, Lucas Smith, Jacob Adams, Diamandis Carolina, Ivanova Olga

Natur- & Humanwissenschaften

ePUB

1,5 MB

DRM: kein Kopierschutz

ISBN-13: 9783756219278

Verlag: Books on Demand

Erscheinungsdatum: 22.05.2022

Sprache: Englisch

Schlagworte: Oslo Syndrome, H63D Syndrome, NTBI, Mutation, Hemochromatosis

Barrierefreiheit: Eingeschränkt zugänglich

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Beschreibung

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.

Autor/in

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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