Juvenile parkinsonism: A patient with possible primary striatal dysfunction

Sakkubai Naidu, Leslie I. Wolfson, Nansie S. Sharpless

Research output: Contribution to journalArticle

Abstract

A 15‐year‐old boy who initially manifested dystonic features and later developed classic parkinsonism is described. Cerebrospinal fluid homovanillic acid levels were normal or slightly elevated both before and after administration of probenecid. The patient responded favorably to treatment with levodopa and carbidopa. The normal or slightly elevated cerebrospinal fluid homovanillic acid levels contrast with the low levels usually seen in adult parkinsonian patients. The data on this patient suggest direct neostriatal involvement rather than depletion of neurons of the substantia nigra. Juvenile parkinsonism may have at least two distinct pathological forms, but they have similar clinical features and a similar response to treatment.

Original languageEnglish (US)
Pages (from-to)453-455
Number of pages3
JournalAnnals of neurology
Volume3
Issue number5
DOIs
StatePublished - May 1978
Externally publishedYes

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Fingerprint Dive into the research topics of 'Juvenile parkinsonism: A patient with possible primary striatal dysfunction'. Together they form a unique fingerprint.

  • Cite this