Skip to main content
. Author manuscript; available in PMC: 2018 Aug 1.
Published in final edited form as: Ann Biomed Eng. 2017 May 30;45(8):1949–1962. doi: 10.1007/s10439-017-1838-0

Table 1. Clinical Characteristics of Participants.

Table A: Children with dystonia. Subject ID; Sex [M: Male; F: Female]; Age [years]; Deep Brain Stimulation (DBS) [Y: yes; N: no]; Diagnosis; Severity of dominant arm (DArm), and Total Score (scores averaged over two raters are based on the Barry-Albright Dystonia Scale (Barry et al., 1999); for each segment the score ranges from 0 - absence of dystonia - to 4 - severe dystonia); Dominant arm; Medications. [*Total Score NOT available]. Table B: Control children. Subject ID; Sex; Age [years]; Dominant arm

(A) Dystonia (B) Control
ID Sex Age DBS Diagnosis Severity Arm ID Sex Age Arm
DArm Total
D1 F 14 Y Idiopathic dystonia DYT1− 2 7 R C1 F 12 L
D2 M 8 N Progressive generalized dystonia (since age 2) idiopathic 1.5 5.5 R C2 F 10 R
D3 M 19 N Torticollis, writer's cramp, leg and foot dystonia from mutation in TTPA (tocopherol transfer protein A) 1.5 6 R C3 F 10 R
D4 F 18 N Generalized secondary dystonia 3 8.5 R C4 F 19 R
D5 M 19 Y Primary dystonia; DYT1+ 1 4.5 R C5 F 20 R
D6 F 10 N Right hemiplegia tremor dystonia 2 5.5 L C6 F 18 R
D7 M 10 N Secondary dystonia due to cerebral palsy 2.5 10 R C7 F 17 R
D8 M 8 N Secondary dystonia due to cerebral palsy 3 9* L C8 M 18 R
D9 M 15 N Generalized secondary dystonia 1 2 L C9 M 18 R