Apert syndrome is a congenital disorder characterized by malformations of the skull, face, hands and feet.

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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.
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.
'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. (August 03, 2003)
[DNA Mozilla]
Last update:
July 15, 2012 at 11:05:06 UTC
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