Occurrence of Parkinson's syndrome in type I Gaucher disease.

نویسندگان

  • O Neudorfer
  • N Giladi
  • D Elstein
  • A Abrahamov
  • T Turezkite
  • E Aghai
  • A Reches
  • B Bembi
  • A Zimran
چکیده

Gaucher disease, the most prevalent glycolipid storage disorder, is classically subdivided into types according to the presence or absence of neurological involvement. Type I has hitherto been considered non-neuronopathic. We present six cases and a review of the literature of Parkinsonian symptoms in type I Gaucher disease patients. The hallmark of this atypical Parkinsonian syndrome is a relatively severe clinical course with early appearance of neurological signs in the 4th to 6th decade of life, aggressive progression of the signs and refractoriness to conventional anti-Parkinson therapy. We discuss the implications of these findings in the light of enzyme replacement therapy for Gaucher disease.

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عنوان ژورنال:
  • QJM : monthly journal of the Association of Physicians

دوره 89 9  شماره 

صفحات  -

تاریخ انتشار 1996