Resumen de Hypodontia and delayed eruption in a patient with a new type of acrocallosal syndrome: report of a case

P. Pérez Prieto, Francisco Javier Silvestre Donat, M. del Campo

• The Acrocallosal syndrome is characterized by macrocephaly, post and/or preaxial polydactyly and syndactyly of fingers or toes, agenesis or hypoplasia of the corpus callosum, growth retardation and severe to profound mental retardation. We report a case of a 14 years old girl diagnosed with a new type of acrocallosal syndrome with hypodontia and delayed eruption. No previous reports link these oral and radiographic findings with this syndrome.