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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)