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DMOZ Internet Directory
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Health
Conditions and Diseases
Congenital Anomalies
Craniofacial Anomalies
Apert Syndrome
8 Sites
Apert syndrome is a congenital disorder characterized by malformations of the skull, face, hands and feet.
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Swedish Apert Syndrome Information
- General information about Apert syndrome with photographs of people with the condition. English version follows Swedish text.
Wikipedia: Apert Syndrome
- Encyclopedia article on this congenital disorder characterized by malformations of the skull, face, hands and feet.
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.
Apert Syndrome
- Frequently asked questions and answers on this disorder.
Krista's Page
- Written by her father, this contains biographical detail about living with Apert syndrome.
What is Apert Syndrome?
- Medical information including definition, major and related features of the condition, genetics.
'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.
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See Also
Genetic Disorders
Health : Conditions and Diseases
331 Sites
Rare Disorders
Health : Conditions and Diseases
7 Sites
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