Cardiac assessment in Wilson’s disease patients based on electrocardiography and echocardiography examination

INTRODUCTION: Wilson’s disease (WD) is a rare genetic disorder that leads to impairments in copper metabolism. Patients principally exhibit liver and neuropsychiatric symptoms, but because copper also accumulates in all body organs, other (typically milder) clinical symptoms can occur. To date, card...

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Detalles Bibliográficos
Autores principales: Buksińska-Lisik, Małgorzata, Litwin, Tomasz, Pasierski, Tomasz, Członkowska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2017
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657248/
https://www.ncbi.nlm.nih.gov/pubmed/31360180
http://dx.doi.org/10.5114/aoms.2017.69728

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657248/
https://www.ncbi.nlm.nih.gov/pubmed/31360180
http://dx.doi.org/10.5114/aoms.2017.69728

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