Microcephaly-cleft palate-abnormal retinal pigmentation syndrome is a rare orofacial clefting syndrome characterized by microcephaly, cleft of the secondary palate and other variable abnormalities, including abnormal retinal pigmentation, facial dysmorphism with hypotelorism and maxillary hypoplasia. Goiter, camptodactyly, abnormal dermatoglyphics and mild intellectual disability may also be associated. There have been no further descriptions in the literature since 1983.
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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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