Dental and craniofacial features associated with GNAS loss of function mutations

ConclusionsPatients with iPPSD2 and maternalGNAS mutations had specific craniofacial alterations and dental abnormalities. These specific defects should be assessed in order to provide appropriate dental and orthodontic care to these patients. (clinical trial registration: 1920371 v 0, French Nationale Data Processing and Liberties Commission - CNIL).
Source: The European Journal of Orthodontics - Category: Dentistry Source Type: research