Article

H63D syndrome (Oslo Syndrome) is clinically the iron sibling of Wilson's disease

2022-06-07

Abstract excerpt

H63D syndrome, now clinically known as Oslo syndrome (synonymous), is considered a very rare disorder that is difficult to recognize due to its multifaceted nature. Even with homozygous mutation of the HFE gene H63D and the simultaneous presence of the typical clinical symptoms, few clinicians dare to care for affected patients. This is inexplicable, because Oslo syndrome (H63D syndrome) looked at on the meta-leve...

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Literature Corpus work: 5ad8791f-0603-51b8-84c4-5057a0678fb6
DOI: 10.22541/au.165459421.16231448/v1

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