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. Author manuscript; available in PMC: 2018 Apr 1.
Published in final edited form as: Mov Disord. 2017 Feb 10;32(4):560–568. doi: 10.1002/mds.26920

TABLE 1.

Demographics of a total of 89 SD patients assigned to different groups based on their phenotypes and putative genotypes

Sporadic versus familial
Sporadic versus familial
ADSD versus ABSD
ADSD versus ABSD
Homogeneous group
Heterogeneous group
Homogeneous group
Heterogeneous group
Sporadic Familial Sporadic Familial ADSD ABSD ADSD ABSD
n 23 (AD) 22 (AD) 30 (7AB/23AD) 29 (7AB/22AD) 30 (SPOR) 30 (SPOR) 37 (30SPOR/7FAM) 37 (30SPOR/7FAM)
Sex, female/male 18/5 19/3 24/6 24/5 23/7 26/4 29/8 31/6
Age (y), mean ± s.d. 56 ± 11 56 ± 15 56 ± 12 56 ± 15 56 ± 12 53 ± 13 56 ± 13 54 ± 12
SD duration, mean ± s.d. 14 ± 11 21 ± 14 16 ± 13 20 ± 14 17 ± 13 15 ± 9 17 ± 12 16 + 11
Age of onset (y), mean ± s.d. 42 ± 13 35 ± 16 40 ± 13 36 ± 17 39 ± 16 38 ± 12 39 ± 17 38 ± 12
Handedness (Edinburgh Inventory) Right
Language Monolingual native English
Cognitive status Mini-Mental State Examination ≥ 27 points
Genetic status Negative for DYT1, DYT6, DYT4, and DYT25

FAM, familial; SPOR, sporadic.