Huntingtons is a genetically inherited disease from a parent. when chromosomes are passed onto a child, the child wont always receive the chromosome containing the gene. But, if they do inherit the gene they will have the disease no matter what, because the disease is dominant. If it was recessive, the child could inherit the disease but not necessarily get the disease.
Autosomal Dominant
An autosomal genetic disorder is Huntington's disease.
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.
One example is Huntington's Disease. Carried on a dominant gene, it causes deterioration of the central nervous system, affecting movement, swallowing, personality, etc.
HD is a genetic disease, and currently cannot be prevented.
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
how is it possible for a person to have dominant genetic disorder? how is it possible for a person to have dominant genetic disorder?
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.
Huntingtons
Yes, autosomal dominant.
by inherited disorder from both or one parent, such as diabetes, cystic fibrosis, parkinsons disease, huntingtons disease etc.
Huntington disease