APERT SYNDROME. Presence of extra finger or fusion of fingers. Most children with Apert Syndrome have some degree of webbing between the fingers or toes. Patients and Methods : Records of 40 children with … Dental problems caused by fusion of teeth sockets. METHODS: This retrospective study examined all Apert syndrome patients from four craniofacial centers who had a panoramic radiograph taken before the age of 16 years. The palate is often high and arched, and sometimes cleft palate occurs. Purpose : Developing teeth are used to assess maturity and estimate age in a number of disciplines. The infant suffering from apert syndrome also suffers from heart, gastrointestinal and urinary problems. A child with Apert syndrome also suffers from midface hypoplasia, bicoronal synostosis, and complex syndactyly of the arms and legs. - Ectopic eruption of upper first permanent molars. Gene mutations are responsible for causing the early fusion of the skull, hand and feet bones. Palate. - About a 1-year dental delay in maturation/eruption in primary and permanent teeth. Apert Syndrome … Causes of Apert Syndrome The purpose of this investigation was to study the dental maturation in children with Crouzon or Apert syndrome compared with nonsyndromic controls. The mid-face has a sunken-in appearance, the upper jaw slopes backward, lower teeth project in front of the upper teeth. Most cases are sporadic. - Shovel-shaped incisors. Successful treatment of patients with Apert syndrome requires an interdisciplinary medical team, including: … There appears to be clinical observations indicating delayed eruption of the permanent teeth in the Apert child. - Enamel opacities and/or hypoplasia. Apert syndrome (acrocephalosyndactyly type I, MIM #101200) is an autosomal dominant disorder that occurs in 6 to 15.5 out of 1 million livebirths . - Supernumerary teeth. Table 1. Apert syndrome is a genetic disorder, characterized by deformities of the skull, face, and limbs affecting an individual’s health, daily function, and social interaction. Knowledge of the most prevalent tooth agenesis patterns may increase our understanding of Apert syndrome by subphenotyping patients with regard to these patterns and by making genotype-phenotype correlations possible.In conclusion, in the present study, the subjects with Apert syndrome were found to exhibit a high prevalence of dental agenesis. Mutations in the gene encoding fibroblast growth factor receptor 2 (FGFR2), located on chromosome 10, account for almost all known cases . Apert syndrome, also called acrocephalosyndactyly, is a genetic syndrome characterized by anomalies of the skull, face and limbs. - Tooth agenesis. Apert syndrome (AS) is an autosomal-dominant inherited disease characterized by premature fusion of bilateral coronal sutures, mid-facial hypoplasia, and symmetric syndactyly of hands and feet. 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