A rare case of first attack psychosis and Wilsons disease
Wilson disease (WD) is an infrequent genetic disorder of copper metabolism (chromosome 13), with decreased transport of copper by hepatic lysosomes due to mutation in the Wilson disease protein (ATP7B) gene. Hence, accumulating copper is primarily affecting the liver, brain, cornea, and kidneys, aft...
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| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Psychopharmacology Association
2017-04-01
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| Colección: | Psychiatry and Behavioral Sciences |
| Materias: | |
| Acceso en línea: | http://www.ejmanager.com/fulltextpdf.php?mno=273317 |
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