Myelopathy secondary to copper deficiency as a complication of treatment of Wilson's disease.

نویسندگان

  • Jesús Lozano Herrero
  • Eduardo Muñoz Bertrán
  • Isabel Ortega González
  • Rosa Gómez Espín
  • María Isabel López Espín
چکیده

Wilson's Disease (WD) is an autosomal recessive disorder of copper metabolism resulting in a pathological accumulation of this metal, initially in the liver and later in other organs, mainly brain. Treatment with copper chelating agents and zinc salts results in a depletion of copper deposits and prevents or reverses the clinical manifestations. Copper deficiency may cause haematological and neurological changes, the latter principally being polyneuropathy and myelopathy. We report a patient with WD who developed a myelopathy associated with a deficiency of copper following prolonged treatment with D-penicillamine and zinc salts.

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عنوان ژورنال:
  • Gastroenterologia y hepatologia

دوره 35 10  شماره 

صفحات  -

تاریخ انتشار 2012