Miller Syndrome

Posted: Sep, 21 2018

Miller Syndrome is a genetic condition, characterized by craniofacial malformations occurring along with abnormalities of the arms, hands and/or feet. Craniofacial abnormalities include underdevelopment of the cheekbones (malar hypoplasia), an abnormally small lower jaw (micrognathia), incomplete closure of the roof of the mouth (cleft palate), small, protruding, ears; and/or absence of tissue (colobomas) from the lower eyelids.