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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Leukodystrophy

Posted by Chavonne Jones On June - 3 - 2008 Subscribe here

Leukodystrophy describes a group of rare genetic disorders that affect the central nervous system. These disorders are progressive in the disruption of the myelin sheath insulating nerve cells. Depending on the type of Leukodystrophy this disorder can be recessive, dominant, or x-linked. Currently there are 34 known variations of this rare genetic disorder. Specific types include: Krabbe Disease, Adrenleukodystrophy, Canavan disease, metachromatic leukodystrophy, and more.

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