Oculopalatocerebral syndrome is characterized by the association of four anomalies: intellectual deficit, microcephaly, palate anomalies and ocular abnormalities.
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Neu-Laxova syndrome
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acrofacial dysostosis, Catania type
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aortic arch anomaly-facial dysmorphism-intellectual disability syndrome
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blepharonasofacial malformation syndrome
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brachydactyly-nystagmus-cerebellar ataxia syndrome
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craniofaciofrontodigital syndrome
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