Robinow syndrome, autosomal dominant (medical condition)

A very rare inherited disorder characterized by short stature and head, face, skeletal and genital abnormalities. The facial appearance is that of a two-month old fetus. The severity and range of symptoms is variable. This dominantly inherited form of Robinow syndrome tends to be milder than the recessive form. See also Dysostosis acral with facial and genital abnormalities