Article

H63D Syndrome renamed Oslo Syndrome

2022-05-20

Abstract excerpt

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 cause, usually after a second hit, rather mild classical hemochromatosis, but it can also cause numerous other disorders of iron metabolism, such as hypotransferrinemia, changes in binding capacity, and others. In addition, it may lead-among other symptoms-to damages of the he...

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Literature Corpus work: 10c4e0f9-ba86-5700-a336-983c8c0dd2e0
DOI: 10.22541/au.165308128.80134531/v1

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