acrodysostosis
ac·ro·dys·os·to·sis
(ak'rō-dis-os-tō'sis), [MIM*101800]Acrodysostosis
An autosomal dominant condition which primarily affects bone and is characterised by ocular hypertelorism, brachycephaly, small upturned broad nose with flat nasal bridge, protruding jaw, short arms and legs with deformities of the hands and feet, possibly with other defects of skin, genitals, teeth, and skeleton. It is usually associated with mental retardation and ear infections.Imaging In early infancy, spotty calcium deposits—stippling in bones—especially in the nose, short bones.