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Table 2 Clinical features and phenotypes of the 33 patients

From: Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy

Evaluation Predominant features Number (%)
At admission Parkinsonism 8 (24)
  Cerebellar ataxia > dysautonomia 24 (73)
  Dysautonomia 1 (3)
At sampling Probable MSA-P 10 (30)
  Possible MSA-P 1 (3)
  Probable MSA-C 21 (64)
  Possible MSA-C 1 (3)
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