Dental and craniofacial features associated with GNAS loss of function mutations.

CONCLUSIONS: Patients with iPPSD2 and maternal GNAS 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). PMID: 31696922 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31696922?dopt=Abstract

Source: European Journal of Orthodontics - November 6, 2019 Category: Dentistry Authors: Le Norcy E, Reggio-Paquet C, de Kerdanet M, Mignot B, Rothenbuhler A, Chaussain C, Linglart A Tags: Eur J Orthod Source Type: research