Characteristics of suppression were determined in 25 participants prospectively recruited for a study of clinical binocular vision tests (19 participants with abnormal binocular vision development from strabismus or amblyopia and 6 participants with normal vision development). Participants were aged from 12 years, and all had a comprehensive vision and intraocular health exam that included previous treatment history, visual acuity (electronic Early Treatment of Diabetic Study e-ETDRS), clinical stereoacuity (Randot Preschool Stereoacuity Test; Stereo Optical Co, Inc., Chicago, IL, USA), ocular alignment (unilateral and prism alternating cover test) and Worth 4 Dot response at 6 m and 33 cm. Classification criteria for normal binocular vision group were best-corrected visual acuity of 0.00 logMAR or better, and 60 sec of arc stereoacuity on Randot Preschool Stereoacuity Test, no suppression on classical 6 m Worth 4 Dot test and no known history of amblyopia or strabismus. Classification criteria for abnormal binocular vision group (BV-abnormal) were a known history of strabismus (with or without amblyopia), or amblyopia (anisometropic, strabismic or combined mechanism). Amblyopia was defined as an interocular difference in best-corrected visual acuity of 0.20 logMAR or more. No participants had coexisting general developmental, systemic, or ocular pathology or congenital abnormality.
Data were collected at the Queensland University of Technology. The study was conducted in accordance with the requirements of the Queensland University of Technology Human Research Ethics Committee. All participants provided written informed consent before the examination, and the protocol adhered to the tenets of the Declaration of Helsinki.