man·dib·u·lo·ac·ral dys·os·to·sis
[MIM*248370] an autosomal recessive disorder, caused by a mutation in the gene LMNA encoding lamin A/C on 1 q. characterized by hypoplastic mandible, dental crowding, acroosteolysis, stiff joints, and atrophy of the skin of the hands and feet; clavicles are hypoplastic, cranial sutures are wide, and multiple sutural bones are present.
Farlex Partner Medical Dictionary © Farlex 2012
man·dib·u·lo·ac·ral dys·os·to·sis
(man-dibyū-lō-akrăl disos-tōsis) [MIM*248370] Disorder characterized by hypoplastic mandible, dental crowding, acroosteolysis, stiff joints, and atrophy of skin of hands and feet.
Medical Dictionary for the Dental Professions © Farlex 2012