Apert syndrome is a congenital disorder characterized by malformations of the skull, face, hands and feet.
  • Apert Syndrome Frequently asked questions and answers on this disorder.
  • CCDD: Apert Syndrome The Center for Craniofacial Development and Disorders at Johns Hopkins University, provides information on this disorder, its causes, diagnosis and treatment.
  • CCDD: Apert Syndrome Information for physicians including clinical manifestations, genetics, pathophysiology, diagnosis and treatment.
  • Contact a Family: Apert Syndrome UK charity for families with disabled children provides information on this rare disorder, its symptoms, causes, how it is diagnosed and treated, inheritance patterns and prenatal diagnosis.
  • Krista's Page Written by her father, this contains biographical detail about living with Apert syndrome.
  • Swedish Apert Syndrome Information General information about Apert syndrome with photographs of people with the condition. English version follows Swedish text.
  • What is Apert Syndrome? Medical information including definition, major and related features of the condition, genetics.
  • Wikipedia: Apert Syndrome Encyclopedia article on this congenital disorder characterized by malformations of the skull, face, hands and feet.

Media publications

  • 'Older Dad' Baby Defect Explained BBC story on the discovery that children born of older fathers are at greater risk of developing Apert, and the mechanism behind that risk. (Published 2003-08-03 00:00:00)

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