Genetic Disorders
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Progeria. Taryn V. Progeria Progeria, also known as Hutchinson-Gilford Progeria Syndrome HGPS, is a rare, fatal genetic condition characterized by an appearance of accelerated aging in children. All children with Progeria die of the same heart disease that affects millions of normal aging adults arteriosclerosis, but instead of occurring at 60 or 70 years of age, these children may . Tay-sachs by Raquel K. Trisomy 18 by Tim O. Downs Syndrome by Izzy L. Izzy L Downs Syndrome In 1856, a phys.CONTENT
This site has the following on the site, "Progeria Progeria, also known as Hutchinson-Gilford Progeria Syndrome HGPS, is a rare, fatal genetic condition characterized by an appearance of accelerated aging in children." Our analyzers noticed that the web site also said " All children with Progeria die of the same heart disease that affects millions of normal aging adults arteriosclerosis, but instead of occurring at 60 or 70 years of age, these children may ." The Website also stated " Trisomy 18 by Tim O. Downs Syndrome by Izzy L. Izzy L Downs Syndrome In 1856, a phys."VIEW MORE BUSINESSES
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Canavan disease is an autosomal recessive gene linked neurological birth disorder in which the white matter of the brain degenerates into spongy tissue filled with microscopic fluid-filled spaces. Canavan disease is caused by mutations in the gene for an enzyme called atrophy. Williams Syndrome by Haley K.
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