Article
Craniofacial and intraoral phenotype of Robinow syndrome forms.
Clinical genetics - 1 Jul 2011
Beiraghi S, Leon-Salazar V, Larson B E, John M T, Cunningham M L, Petryk A, Lohr J L
Abstract excerpt
Robinow syndrome (RS) is a rare genetic condition with two inheritance forms, autosomal dominant RS (DRS) and autosomal recessive RS (RRS). The characteristic features of this syndrome overlap in both inheritance forms, which make the clinical differential diagnosis difficult, especially in isolated cases. The objective of this study was to identify differences in the craniofacial and intraoral phenotype of...
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