Huntington's disease is a disorder passed down through families in which nerve cells in the brain waste away, or degenerate. Not a mutation. Amber
Autosomal Dominant
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.
Huntington's disease is a genetic disorder that causes the progressive breakdown of nerve cells in the brain. It leads to various physical and mental symptoms, including involuntary movements, cognitive impairment, and psychiatric issues. There is currently no cure for Huntington's disease.
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
genetic disorder
huhuhhuhuhuuh
Huntington's disease is a genetic disorder caused by a mutation in the HTT gene, which encodes the protein huntingtin. This mutation involves an abnormal expansion of CAG repeats in the gene, leading to the production of a toxic form of the huntingtin protein that gradually damages neurons in the brain. The disorder follows an autosomal dominant inheritance pattern, meaning that an individual only needs one copy of the mutated gene from either parent to develop the disease. As a result, it typically manifests in mid-adulthood and progressively leads to motor, cognitive, and psychiatric symptoms.
It's a gene mutation. And it is different for each organ.
A mutation in the gene makeup of the organism.
Huntingtons disease is a genetic/inherited diesease. It is caused by a faulty allele (a dominant one), which can be inherited by parents. Spontanoius mutations may also occur which would cause the faulty gene and therefore huntingtons disorder.
A mutation in the gene makeup of the organism.
Sickle cell anemia.