Hungtington disease is a trinucleotide repeat genetic disorder, in which you have extra repeats of CAG in your gene coding for the hungtin protein. If you have more than 35 repeats you get the phenotype (symptoms), and it shows anticipation, which means that as the disease is passed on from generation to generation the repeats increase, hence the severity of the disease. It is quite rare, but the exact incidence is hard to estimate, because people carrying 30 repeats are asymptomatic. Hope this helps
Among others, Huntington's Disease.
Huntington disease
Huntington's disease is a genetic disorder. In other words, it runs in the family. It is not contagious. You are born with it and the symptoms show up as you age.
Mutation, migration, and genetic drift
Children of a parent that has HD. It is a genetic disease- the only way to get it is to inherit it.
Hungtington's disease is a dominant mutation in the gene that codes for the protein 'Huntington' It only affects a single gene, the remainder of the chromosome is unaffected and therefore it is not a chromosomal abnormality
Huntington's disease is not contagious as it is a genetic disorder. It is passed down from parents.
This means that you have a genetic disease where as your DNA suppresses certain proteins in your body, thus either 1: giving you a deadly mutation somewhere on the body or 2: killing you I think?
Yes, autosomal dominant.
Nope it's genetic
Several diseases, including Huntington's, have a genetic screening test to identify the presence of the gene that causes Huntington's. Please visit the website for the Huntington's Disease Society of America for some good information.
ONE is Huntington's Disease.
Achrondoplasia (dwarfism) is one. Another is Huntington's disease.
Among others, Huntington's Disease.
It is a genetic disease. You can only "catch" it by inheriting the gene for it.
page 314 Huntington's disease is lethal GENETIC DISORDER caused by a rare dominant allele. It's not a chromosonal disease, it is a genetic disorder. D
Around 1 in 10,000 people are estimated to develop Huntington's disease, a rare genetic disorder. It is caused by a mutation in the HTT gene on chromosome 4.