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Delayed-onset progressive movement disorders after static brain lesions.

Publication ,  Journal Article
Scott, BL; Jankovic, J
Published in: Neurology
January 1996

We studied 53 patients (64% females) with static brain lesions who developed progressive movement disorders. Of these, 50 (94%) had dystonia, 17 (32%) tremor, eight (15%) parkinsonism, seven (13%) myoclonus, and three (6%) chorea. The precipitating insults included perinatal hypoxia/ischemia in 22 (42%), stroke in 12 (23%), head injury in eight (15%), encephalitis in eight (15%), and carbon monoxide poisoning, kernicterus, and radiation necrosis in one patient (2%) each. Among the 30 patients with initial insult occurring at age 2 years or younger (Infant group), distribution of dystonia at follow-up was focal in three (10%), segmental in eight (27%), unilateral in 10 (33%), and generalized in nine (30%). The mean latency between the original injury and onset of movement disorder was 25.5 +/- 16.7 years. Among the nine patients who developed dystonia after an insult occurring between ages 6 and 17 (Childhood group), the distribution of dystonia at follow-up was segmental in two (33%) and unilateral in seven (78%); the mean latency of dystonia onset was 4.9 +/- 7.8 years. Of the 14 patients in the Adult group (injury at age 25 or older), 11 developed dystonia, two developed parkinsonism, and one had carbon monoxide encephalopathy and parkinsonism. The distribution of dystonia in the 11 patients at follow-up was segmental in three (27%) and unilateral in eight (73%). The mean latency of movement disorder onset in the 14 patients of the Adult group was 2.5 +/- 4.9 years. No individuals in the Childhood or Adult groups became left-hand dominant; by comparison, nine of the 30 individuals in the Infant group became left-handed. In conclusion, brain injury at a young age is associated with a longer latency to onset of subsequent movement disorder, a greater tendency to development of generalized dystonia, and a greater probability of altered handedness. These tendencies may result from differences in age-related neuroplasticity.

Duke Scholars

Published In

Neurology

DOI

ISSN

0028-3878

Publication Date

January 1996

Volume

46

Issue

1

Start / End Page

68 / 74

Location

United States

Related Subject Headings

  • Time Factors
  • Neurology & Neurosurgery
  • Movement Disorders
  • Middle Aged
  • Male
  • Infant
  • Humans
  • Female
  • Child, Preschool
  • Child
 

Citation

APA
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Scott, B. L., & Jankovic, J. (1996). Delayed-onset progressive movement disorders after static brain lesions. Neurology, 46(1), 68–74. https://doi.org/10.1212/wnl.46.1.68
Scott, B. L., and J. Jankovic. “Delayed-onset progressive movement disorders after static brain lesions.Neurology 46, no. 1 (January 1996): 68–74. https://doi.org/10.1212/wnl.46.1.68.
Scott BL, Jankovic J. Delayed-onset progressive movement disorders after static brain lesions. Neurology. 1996 Jan;46(1):68–74.
Scott, B. L., and J. Jankovic. “Delayed-onset progressive movement disorders after static brain lesions.Neurology, vol. 46, no. 1, Jan. 1996, pp. 68–74. Pubmed, doi:10.1212/wnl.46.1.68.
Scott BL, Jankovic J. Delayed-onset progressive movement disorders after static brain lesions. Neurology. 1996 Jan;46(1):68–74.

Published In

Neurology

DOI

ISSN

0028-3878

Publication Date

January 1996

Volume

46

Issue

1

Start / End Page

68 / 74

Location

United States

Related Subject Headings

  • Time Factors
  • Neurology & Neurosurgery
  • Movement Disorders
  • Middle Aged
  • Male
  • Infant
  • Humans
  • Female
  • Child, Preschool
  • Child