oculocerebral-hypopigmentation syndrome /ok′yəlō′- sərē′brəl/ [L, oculus, eye + cerebrum, brain] , an autosomal-recessive syndrome marked by cutaneous hypopigmentation, microphthalmos, small opaque corneas, gingival hypertrophy, and cerebral defect manifested by spasticity, mental and physical disabilities, and athetoid movements. Also called Cross syndrome.
