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oculocerebral-hypopigmentation syndrome |
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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. Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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