Assessment of neurological symptoms and associated factors in patients with Wilson’s disease in Southwest China
Abstract Background Wilson’s disease is an inherited genetic disorder of hepatic copper metabolism characterized by hepatic, neurological, and psychiatric manifestations. Patients with neurological symptoms manifest remarkable variability regarding type and severity. This study aimed to characterize...
Saved in:
| Main Authors: | , , , , , , , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2025-07-01
|
| Series: | Orphanet Journal of Rare Diseases |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13023-025-03874-2 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|