oculocerebral-hypopigmentation syndrome

oculocerebral-hypopigmentation syndrome

[ok′yəlō′- sərē′brəl]
Etymology: 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 retardation, and athetoid movements. Also called Cross syndrome.
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