Karantzoulis S

ORCID: 0000-0001-9707-517X · 1 paper in corpus
2021
Orphanet journal of rare diseases ·doi:10.1186/s13023-021-02059-x

BackgroundWilson disease (WD) is a rare disease wherein copper accumulates in tissues, leading to hepatic degeneration, neurological impairments, and psychiatric symptoms. This study aimed to characterize the patient experience of WD and de…