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Huntington's disease primarily affects neurons in the brain, particularly in the basal ganglia, which is involved in movement control and coordination. The disease is characterized by the progressive degeneration of medium spiny neurons, leading to the hallmark symptoms of motor dysfunction, cognitive decline, and psychiatric issues. The underlying cause is a genetic mutation in the HTT gene, resulting in the production of a toxic form of the huntingtin protein that disrupts neuronal function and survival.
What else can I help you with?
Compare the inheritance of Huntingtons disease with the inheritance of sickle cell anemia?
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.
Symptoms of huntingtons disease?
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
Is huntingtons disease monosomy or trisomy?
Monosomy
Can night sweats be a symptom of huntingtons disease?
No.
Are aspergers syndrome and huntingtons disease connected?
No.
Is cystic fibroses linked with huntingtons disease?
No
What are ten genetics diseases?
huntingtons tay sachs cystic fibrosis downs syndrome sickle cell anemia color blindness turner syndrome klinefelter disease alzheimers disease crohns disease
Can Huntingtons Disease be diagnosed after birth with a simple blood test?
Genetic testing can determine this (which is more involved than just a simple blood test).
How many people have huntingtons disease?
One in ten thousand have Huntington's disease.
How is huntingtons disease inherited?
Its Passed On From Your Parents Its Inherited
What is a treatment for huntingtons disease?
medication and anti deprassants
Is Parkinsons chorea related to Huntingtons disease in men?
No.
