Neurological features and management of Wilson disease in children: an evaluation of 12 cases

AIM: Wilson’s disease is an autosomal recessive disorder of copper metabolism which leads to copper overload in different tissues of the body. The aim of this study was to present the neurologic features of Wilson’s disease and to assess the clinical course of neurological findings in children recei...

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Dades bibliogràfiques
Publicat a:Turk Pediatri Ars
Autors principals: Bayram, Ayşe Kaçar, Gümüş, Hakan, Arslan, Duran, Özçora, Güldemet Kaya, Kumandaş, Sefer, Karacabey, Neslihan, Canpolat, Mehmet, Per, Hüseyin
Format: Artigo
Idioma:Inglês
Publicat: Turkish Pediatrics Association 2016
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4829162/
https://ncbi.nlm.nih.gov/pubmed/27103860
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2016.3080
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