CareLit Fachartikel

Wilson's disease and multiple sclerosis

P Günther, W Hermann, A Wagner · Klinische Neurophysiologie · 2009 · Heft 03

Dokument
1165734
CareLit-ID
Jahr
2009
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Klinische Neurophysiologie
Autor:innen
P Günther, W Hermann, A Wagner
Ausgabe
Heft 03 / 2009
Seiten
–
Erschienen: 2009-03-13 00:00:00
ISSN
1434-0275

Zusammenfassung

Introduction: Wilson's disease is a rare autosomal recessive disorder of hepatic copper transport leading to hepatic but also to highly variable neurological symptoms with extrapyramidal motor and cerebellar manifestation. Overlap of symptoms and also of results of multimodal evoked potentials to other central nervous system disorders as Multiple Sclerosis occur and sometimes complicate the diagnosis. Case report: We report a 38 year old male patient who was diagnosed with a hepatic form of Wilson's disease at age 12 and with Multiple Sclerosis at age 36. Intravenous radio copper test confirmed the diagnosis of…

Schlagworte

Diagnosis After Klinische Neurophysiologie