Dental and cranio-facial aspects of Williams Syndrome

نویسندگان

  • E. DEFRAIA
  • G. BARONI
  • C. INNOCENTI
چکیده

Williams Syndrome is a rare genetic disorder caused by a hemizygote micro-deletion mapped to the long arm of chromosome 7.The main symptoms are a distinctive facial appearance, psychomotor retardation with friendly behaviour and cardiovascular malformations. This case report describes the anomalies of the cranio-facial complex and the cephalometric aspects which are characteristic of this syndrome,

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تاریخ انتشار 2007