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

• P. Pérez-Priego ^[1] ; FJ Silvestre-Donat ^[1] ; M del Campo ^[1]
  1. [1] Universitat de València

     Universitat de València

     Valencia, España

     
• Localización: Cuidados odontológicos especiales: Revista de la Sociedad Española de Odontoestomatología, ISSN 1135-030X, Vol. 5, Nº. Extra 1 (Enero-Abril), 1998 (Ejemplar dedicado a: Special Needs in Dentistry), págs. 13-15
• Idioma: inglés
• Texto completo no disponible (Saber más ...)
• Resumen

  • 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.