Microcephaly-cleft palate syndrome

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.

Also known as: Halal syndrome, microcephaly cleft palate autosomal dominant, microcephaly-cleft palate-abnormal retinal pigmentation syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly-cleft palate syndrome itself.