Fatal Familial Insomnia

fatal familial insomnia fatal Familial Insomnia by: Ann M. Akroush Fatal familial insomnia is a genetic disorder. It manifests itself by many symptoms collectible to the degeneration of a certain part of the brain, the thalamus. The disease in any case resolvents in the formation of amyloid plaques. This is the build up of a waxy substance made of proteins associated with polysaccharides. The disease is a result of a mutation of a shape protein that is associated with brain tissue. This is the prion protein. In the case of fatal familial insomnia, the mutation occurs 178 amino acids into the normal protein.

Were an asparagine should be, an aspartic acid is instead. This disease is an autosomal dominant, which means that both sexes atomic number 18 affected and there are no carriers. If an individual inherits the variant gene, that individual will at some point die hard the disease. In the case of fatal familial insomnia, the affected discipline of the brain is the area responsible for sleep, the thal...If you want to get a full essay, order it on our website: Ordercustompaper.com

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