Huntington's disease is an autosomal dominant disorder. This means that a person only needs one copy of the mutated gene, inherited from either parent, to develop the disease. As a result, each child of an affected individual has a 50% chance of inheriting the condition.
Autosomal Dominant
Huntingtons Disease
Huntington's Disease is an Autosomal Dominant Trait, meaning that only one parent needs to pass the disease for the offspring to inherit it.
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.
the man has huntingtons disease
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.
No, it is autosomal dominant.
Huntingtons disease is Autosomal dominant, i.e. a 50% chance of inheritance if one parent has the gene. Where as sickle cell anemia is autosomal recessive. This gives a 25% chance of inheritance if both parents are carriers.
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
Monosomy