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Screening of Wilson’s disease in a psychiatric population: difficulties and pitfalls. A preliminary study
BACKGROUND: Wilson’s disease (WD) is a rare autosomal-recessive, inherited disorder caused by a mutation in the copper-transporting gene ATP7B affecting the liver and nervous system. About 30% of patients with WD may initially present with psychiatric symptoms, and diagnosis can be difficult to esta...
Autores principales: | Demily, Caroline, Parant, François, Cheillan, David, Broussolle, Emmanuel, Pavec, Alice, Guillaud, Olivier, Restier, Lioara, Lachaux, Alain, Bost, Muriel |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379609/ https://www.ncbi.nlm.nih.gov/pubmed/28392828 http://dx.doi.org/10.1186/s12991-017-0142-6 |
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