Ontology highlight
ABSTRACT:
SUBMITTER: Raviraj J
PROVIDER: S-EPMC5504876 | biostudies-other | 2017 May-Jun
REPOSITORIES: biostudies-other
Dental research journal 20170501 3
Achondroplasia is the most common cause of dwarfism, which is inherited as an autosomal dominant disorder, caused by genetic mutation in fibroblast growth factor 3, leading to defective maturation of chondrocytes. It is known to be associated with various oral and dental manifestations such as delayed dental development, midfacial hypoplasia and constricted maxilla with a relatively large mandible, resulting in skeletal/dental Class III malocclusion, posterior crossbite, anterior reverse jet and ...[more]