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No. It's an inherited disease. The gene is dominant so basically if you have it, 50% of your children will inherit it as well which can particularly devastating since the symptoms don't appear until the 30's or 40's. So theoretically you can have children that are teenagers by the time you find out, and 50% of them will become afflicted as well.

ERROR, each of your children has a 50% chance of inheriting the gene. ALSO, there is Jhd, where children can get it... usually when HD is inherited from the father... but not always. Children as young as 2 have been known to have it. Sadly I have known too many children to die of Jhd.

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9y ago

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Related Questions

Is huntington's disease chromosomal error or a multifactorial trait?

Huntington's disease is primarily caused by a genetic mutation, specifically an expansion of CAG repeats in the HTT gene located on chromosome 4. This mutation leads to the production of a toxic protein that causes neurodegeneration. While there are some environmental factors that may influence the onset and progression of the disease, it is not considered a multifactorial trait in the same way that conditions like heart disease or diabetes are. Thus, Huntington's disease is fundamentally a chromosomal error rather than a multifactorial condition.


Why is Huntington's disease dominant in inheritance patterns?

Huntington's disease is dominant in inheritance patterns because only one copy of the mutated gene is needed to develop the disease. This means that if a person inherits the mutated gene from just one parent, they will likely develop Huntington's disease.


Is huntington disease an autosomal disorder?

Yes. HD is a disease of autosomal dominant inheritance.


What causes moyamoya disease?

The cause of moyamoya disease is unknown. Possible explanations for the disorder include injuries to the brain, infection, multifactorial inheritance, genetic factors, or other causes


Which of the following is an example of an autosomal dominant disease A Huntington's disease and neurofibromatosis type 1 or B Alzheimer's Disease and Heart Disease?

A. Huntington's disease and neurofibromatosis type 1 are examples of autosomal dominant diseases. These conditions are caused by a single copy of a mutated gene on an autosome (non-sex chromosome) and can be passed down from one affected parent to their offspring with a 50% chance of inheritance.


What are true statements about Huntington's Disease?

In the United States, about 1 in every 30,000 people has Huntington's Disease.


What is a similar disease to Huntington's disease?

Huntington's Chorea


How did George Huntington discover Huntington's disease?

He didn't "discover" it, but he was the first to publish an accurate description of the disease that now bears his name. He was the son of a physician, and then himself becamse a physician, who had the opportunity to observe several generations of people with the disease, which allwed him to draw conclusions about inheritance as well as symptoms.


What is multifactorial transmission?

This occurs when environmental factors interact with genetic factors to produce traits. The term multifactorial means many factors. Traits that involve multiple genes and complicated patterns of inheritance are said to be exhibiting multifactorial transmission.


What is the genotype of the mother in the Huntington disease having a dominant of DD or Dd inheritance pattern?

In Huntington's disease, which follows a dominant inheritance pattern, the mother's genotype could either be homozygous dominant (DD) or heterozygous (Dd). If she has the disease, she must have at least one dominant allele, so her genotype cannot be homozygous recessive (dd). Therefore, her possible genotypes are DD or Dd, which both indicate she has the potential to pass the disease on to her offspring.


Is Huntington's disease found in women of Jewish decent?

ANYONE can get Huntington's disease.


Graph showing how many people have huntington's disease?

graph of huntington disease