This website is committed to genetics education awareness. To obtain a better understanding about genetic revolution, we provide the history of genetics. The latest information on all human genetic disorders from Achondroplasia to Wilson's disease is available. Other areas of focus include: dna and rna sequencing, stem cell research and therapy, genetic testing and screening, genetic selection, genes and behavior, mental health, gene therapy, cytocogenetics, pharmacogenetics, xenotransplantation, cloning, ethical, legal, and social issues in medical genetics.


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Archive for the ‘Apert Syndrome’ Category

Apert Syndrome

Posted by Chavonne Jones On March - 15 - 2008 ADD COMMENTS Subscribe here

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Apert syndrome is an autosomal dominant disorder. One of the major symptoms is a premature closure of the skull bones leading to facial distortion with an unusually tall skull. Individuals with apert syndrome also suffer from syndactyly, which is the fusion of the fingers and toes. The hand appears mitten-shaped due to the finger infusion.


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