What are the symptoms for Huntigtons disease?!
Question: What are the symptoms for Huntigtons disease!?
what is it!?
what are its symptoms!?
im only 14, so complicated answers will just confuse me!.Www@Answer-Health@Com
what are its symptoms!?
im only 14, so complicated answers will just confuse me!.Www@Answer-Health@Com
Answers:
The symptoms of Huntington's disease are sometimes overlooked!. This is because they are mild at first and people without the disease can have the same symptoms!. People who have Huntington's disease sometimes have problems for a long time before they find out that they have the condition!.
Early symptoms include:
mild tremor
clumsiness
lack of concentration and irritability
difficulty remembering things
mood changes, including depression
aggressive antisocial behaviour
Over time the symptoms become progressively worse!. Eventually, full-time nursing care will be needed!. Later symptoms fall into three categories:
Physical symptoms
Physical symptoms include chorea (involuntary movements of the limbs, face and body)!. Chorea may lead to difficulty walking, speaking and swallowing!. People often lose weight because of difficulty eating and by burning more calories due to the continuous movement!. The ability to coordinate movement gets gradually worse as the disease progresses!.
Emotional symptoms
Emotional symptoms include depression, not only because of the burden of having a progressive disorder, but as a direct result of the damage to certain brain cells!. You may become frustrated at being unable to work or do previously simple tasks!. You may behave stubbornly, and have mood swings!. People with Huntington's may also become more irritable and antisocial than usual, or have less inhibitions!.
Cognitive symptoms
Cognitive symptoms include a loss of drive and initiative!. People with Huntington's may appear to be lazy or uninterested in life, spending days doing little or neglecting personal hygiene!. You may also lose the ability to organise yourself!. This is because planning skills and the ability to do more than one task at once deteriorate!. In the later stages, you may get memory loss and be less able to understand speech!.
The behavioural changes that occur are often the most distressing for you, your family and your carers!. A previously full and active life may be lost with a gradual reduction in independence and mobility!. At the same time, your personality can become gradually more self-centred and unmotivated, straining personal relationships!.
Causes
Huntington's disease is caused by a faulty gene that runs in families!. The gene, which was discovered in 1993, produces a protein called Huntingtin!. Scientists are still researching how the faulty gene causes the disease!.
Most genes in the body are present in two copies: one from your mother and one from your father!. The gene that causes Huntington's disease is dominant!. This means that if you inherit a copy of this gene from either parent, you will go on to develop the disease at some point in your life!.
If you have one parent with Huntington's disease you have a 50 percent chance of inheriting the faulty gene!. The risk is 50 percent for each child!. It isn't altered by gender or whether brothers and sisters are affected!. Only people who have the faulty gene can pass it on to their children!.
Occasionally there is no family history of the condition!. This may be because previous generations weren't diagnosed - either because of early death from other causes, or loss of contact through adoption!.
Huntington's disease causes progressive damage to cells in areas of your brain called the basal ganglia and cerebral cortex!. These areas are involved in the control of movement, planning, motivation and personality!.
Juvenile Huntington's disease
A juvenile form of Huntington's disease, which develops before the age of 20, also exists!. About five percent of people with Huntington's disease are affected by the condition when this young!. The symptoms are similar to those of adult Huntington's, but muscular rigidity is more likely to occur!. Epilepsy - which causes fits - is also more common among those with juvenile Huntington's disease compared with adults who have the condition!.
Treatment
Although there is currently no cure for Huntington's disease, there are drugs to help manage some of your symptoms!. There are medicines that can reduce the involuntary movements, and antidepressant medicines may alleviate depression!. Mood stabilisers and antipsychotic drugs can help with some of the emotional disturbances!.
Counselling can also be helpful, both for you and your family!. Dieticians can advise on adequate calorie and nutrient intake to stop weight loss!.
Www@Answer-Health@Com
Early symptoms include:
mild tremor
clumsiness
lack of concentration and irritability
difficulty remembering things
mood changes, including depression
aggressive antisocial behaviour
Over time the symptoms become progressively worse!. Eventually, full-time nursing care will be needed!. Later symptoms fall into three categories:
Physical symptoms
Physical symptoms include chorea (involuntary movements of the limbs, face and body)!. Chorea may lead to difficulty walking, speaking and swallowing!. People often lose weight because of difficulty eating and by burning more calories due to the continuous movement!. The ability to coordinate movement gets gradually worse as the disease progresses!.
Emotional symptoms
Emotional symptoms include depression, not only because of the burden of having a progressive disorder, but as a direct result of the damage to certain brain cells!. You may become frustrated at being unable to work or do previously simple tasks!. You may behave stubbornly, and have mood swings!. People with Huntington's may also become more irritable and antisocial than usual, or have less inhibitions!.
Cognitive symptoms
Cognitive symptoms include a loss of drive and initiative!. People with Huntington's may appear to be lazy or uninterested in life, spending days doing little or neglecting personal hygiene!. You may also lose the ability to organise yourself!. This is because planning skills and the ability to do more than one task at once deteriorate!. In the later stages, you may get memory loss and be less able to understand speech!.
The behavioural changes that occur are often the most distressing for you, your family and your carers!. A previously full and active life may be lost with a gradual reduction in independence and mobility!. At the same time, your personality can become gradually more self-centred and unmotivated, straining personal relationships!.
Causes
Huntington's disease is caused by a faulty gene that runs in families!. The gene, which was discovered in 1993, produces a protein called Huntingtin!. Scientists are still researching how the faulty gene causes the disease!.
Most genes in the body are present in two copies: one from your mother and one from your father!. The gene that causes Huntington's disease is dominant!. This means that if you inherit a copy of this gene from either parent, you will go on to develop the disease at some point in your life!.
If you have one parent with Huntington's disease you have a 50 percent chance of inheriting the faulty gene!. The risk is 50 percent for each child!. It isn't altered by gender or whether brothers and sisters are affected!. Only people who have the faulty gene can pass it on to their children!.
Occasionally there is no family history of the condition!. This may be because previous generations weren't diagnosed - either because of early death from other causes, or loss of contact through adoption!.
Huntington's disease causes progressive damage to cells in areas of your brain called the basal ganglia and cerebral cortex!. These areas are involved in the control of movement, planning, motivation and personality!.
Juvenile Huntington's disease
A juvenile form of Huntington's disease, which develops before the age of 20, also exists!. About five percent of people with Huntington's disease are affected by the condition when this young!. The symptoms are similar to those of adult Huntington's, but muscular rigidity is more likely to occur!. Epilepsy - which causes fits - is also more common among those with juvenile Huntington's disease compared with adults who have the condition!.
Treatment
Although there is currently no cure for Huntington's disease, there are drugs to help manage some of your symptoms!. There are medicines that can reduce the involuntary movements, and antidepressant medicines may alleviate depression!. Mood stabilisers and antipsychotic drugs can help with some of the emotional disturbances!.
Counselling can also be helpful, both for you and your family!. Dieticians can advise on adequate calorie and nutrient intake to stop weight loss!.
Www@Answer-Health@Com
Here is a good page, seems uncomplicated:
http://www!.medicinenet!.com/huntington_di!.!.!.
Basically, the main symptoms are dementia (decreased ability to think clearly, poor memory, concentration, ability to learn new things) and chorea which is a kind of irregular twitch and tremor (chorea is a greek word meaning dance - this is because the person experiences short, irregular muscle twitches which jerk the hands and legs around)!.Www@Answer-Health@Com
http://www!.medicinenet!.com/huntington_di!.!.!.
Basically, the main symptoms are dementia (decreased ability to think clearly, poor memory, concentration, ability to learn new things) and chorea which is a kind of irregular twitch and tremor (chorea is a greek word meaning dance - this is because the person experiences short, irregular muscle twitches which jerk the hands and legs around)!.Www@Answer-Health@Com
Huntington's Disease is hereditary!. That means you can only have it if one of your parents has it!. Not all children will be affected though!.
If you are worried then you should talk to your parents or your Doctor!.
My friend has Huntington's; he is 51 now and his symptoms are still quite mild!.
Try not to worry hun!. Just please talk to someone!.Www@Answer-Health@Com
If you are worried then you should talk to your parents or your Doctor!.
My friend has Huntington's; he is 51 now and his symptoms are still quite mild!.
Try not to worry hun!. Just please talk to someone!.Www@Answer-Health@Com
Not being able to spell it properly
just joking - have a look at this link -
http://www!.healthline!.com/adamcontent/hu!.!.!.Www@Answer-Health@Com
just joking - have a look at this link -
http://www!.healthline!.com/adamcontent/hu!.!.!.Www@Answer-Health@Com
You need to look it up online!.!.!.Huntingtons disease isnt that easy to explain!.!. try bbc sites or nhs on google searches xWww@Answer-Health@Com