Miller Syndrome

September 21, 2018 6:49 pm Published by

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.

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