Manic episode induced by discontinuance of D-penicillamine treatment in Wilson’s disease
Wilson’s disease (WD) is a rarely seen autosomal recessive inherited genetic disease of copper metabolism, which leads to various hepatic, orbital and neuropsychiatric disorders. Neuropsychiatric symptoms are due to degeneration that results from the acccumulation of copper in the neurons of the br...
Wedi'i Gadw mewn:
| Prif Awduron: | , |
|---|---|
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Mesut Çetin
2021-02-01
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| Cyfres: | Psychiatry and Clinical Psychopharmacology |
| Pynciau: | |
| Mynediad Ar-lein: | https://psychiatry-psychopharmacology.com/index.php/pub/article/view/839 |
| Tagiau: |
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
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