Published June 6, 2022
| Version 2.9
Journal article
Open
H63D syndrome (Oslo Syndrome) is clinically the iron sibling of Wilson's disease
Authors/Creators
- 1. LCG Greece Research
- 2. Jewish University of Colorado
Description
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-level is nothing more than Wilson disease caused by NTBI iron.
Files
Oslo Syndrom and Morbus Wilson.pdf
Files
(744.6 kB)
| Name | Size | Download all |
|---|---|---|
|
md5:6b4efb37a84abe8ff918ad5ac3c785f3
|
744.6 kB | Preview Download |