Enfermedad de Wilson : revisión del tema

ABSTRACT: Wilson’s disease is an autosomal recessive disorder caused by mutations in the ATP7B gene that lead to an abnormal metabolism of copper, resulting in the accumulation of this element in several organs and tissues. Its diagnosis is based on the combination of the clinical picture with vario...

Full description

Autores:

Espinoza Herrera, Yeinis Paola
Muñoz Ruiz, Luis Manuel
Restrepo Gutiérrez, Juan Carlos

Tipo de recurso:

Review article

Fecha de publicación:

2010

Institución:

Universidad de Antioquia

Repositorio:

Repositorio UdeA

Idioma:

spa

OAI Identifier:

oai:bibliotecadigital.udea.edu.co:10495/12662

Acceso en línea:

http://hdl.handle.net/10495/12662

Palabra clave:

Enfermedad de Wilson
Degeneración Hepatolenticular
Metabolismo del cobre
Quelantes

Rights

openAccess

License

Atribución-NoComercial-CompartirIgual 2.5 Colombia (CC BY-NC-SA 2.5 CO)