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
An autosomal genetic disorder is Huntington's disease.
One example is Huntington's Disease. Carried on a dominant gene, it causes deterioration of the central nervous system, affecting movement, swallowing, personality, etc.
Deletion
Chromosomal Dna.
Chromosomal defects in offspring. Because no genetic material is lost with inversion of genetic material, individuals often have no obvious physical effects. The major risk with the inversion of genetic material is that offspring of these individuals may have more severe chromosomal abnormalities.
Autosomal Dominant
HD is a genetic disease, and currently cannot be prevented.
Huntingtons
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.
by inherited disorder from both or one parent, such as diabetes, cystic fibrosis, parkinsons disease, huntingtons disease etc.
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
Genetic testing can determine this (which is more involved than just a simple blood test).
Huntington's is a genetic disease meaning that it is inherited to offspring of effected parents. If one of your biological parents have it you are at risk. I would ask my doctor for genetic testing to see if I had it.
Down's syndrome is a serious genetic disease caused by chromosomal problems. hope i could help.
Monosomy
No.