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Table 1 Main demographical, clinical and molecular characteristics of the enrolled subjects

From: Heritability of saccadic eye movements in spinocerebellar ataxia type 2: insights into an endophenotype marker

Variable

SCA2 patients

(N = 48)

Preclinical carriers

(N = 25)

Healthy controls

(N = 24)

Gender (female/male)

19/29

16/9

15/9

Age (years)

41.35 ± 9.79

(18–69)

36.88 ± 9.14

(24–61)

41.13 ± 11.05

(20–63)

Age at onset (years)

30.06 ± 9.06

(9–60)

NA

NA

Disease duration (years)

11.71 ± 6.08

(3–29)

NA

NA

SARA score

15.81 ± 5.59

(6–30)

0.76 ± 0.66

(0–2)

0

Unexpanded CAG repeat (units)

22.08 ± 0.92)

(19–27)

22.84 ± 1.93

(22–29)

22.54 ± 1.76

(20–30)

Expanded CAG repeat (units)

39.81 ± 2.92

(35–47)

35.76 ± 1.90

(32–39)

NA

  1. For quantitative variables the mean ± standard deviation and range (in parenthesis) are shown
  2. NA Not applicable, N Number of subjects, SARA Scale for the assessment and rating of ataxia