During Huntington’s diseases (HD) is a progressive neurodegenerative disease, which is transmitted to the genetics of Father to the child.Classic symptoms include uncontrolled movements on the face, trunk, weapons and feet, as well as problems that think clearly and change humor, such as anxiety, depression and irritability.Although Huntington’s disease can not be cured or decreasing, some symptoms can be controlled with medications.
Images Lafor / Getty
Symptoms of Huntington’s disease
250,000 People in the United States have or develop Huntington’s disease. The symptoms generally begin between the ages of 30 and 50, although they are juvenile HD approaching people up to 20 years.
The symptoms of Huntington’s disease slowly degraded over time and tend to vary depending on the stage of the disease:
The Early HD symptoms include:
is difficult new things or to make
involuntary movement or twitch
Coordination calls A> Memory cutter problems
How Huntington’s disease progresses in theAverage stage There are problems with swallowing, talking, walking, memory and concentrating on tasks. Weight loss and malnutrition are common.
Classic automatic movements (Chorea) HD can become very pronounced and significantly interfere with daily operation.
A person can also develop some obsessive behaviors.
Late Step HD
Symptoms of the disease in the late stages, consist In disability walking or talking is very careful.
Instead of the task, a person can have rigidity, decelerated movements (called Bradykinesia), and dynamic. People who have the late stage HD have a high risk of thinking.
pneumonia is the most common cause of death associated with Huntington’s disease.
With Huntington’s disease, a defective gene (called GEN HTT) creates a mutant protein that leads To death nerve cells in the human brain.
Almost all cases of hereditary HD, and the disease is inherited into a self-dominant pattern. This means that if your parent or your mother HD HD has a 50% probability of HD gene.
If you inherit a defective or modified HTT gene, it is most likely that it will develop Huntington’s disease. However, if you do not do this, HD should not be developed. The elimination of rare cases when the
mutation of novo in HD HD HD arises.In these cases, the disease can not be traced for another person in the family.
The Disease Diagnosis of Huntington begins with the history of the disease and is confirmed by blood tests to search the HTT gene.
In addition to the request for possible symptoms of Huntington’s disease, your supplier Medical care wants to obtain a detailed history of the family.Sometimes, old medical recordings or opening reports are needed to complete this.
Analysis of genetic blood
if symptoms of HD subject or have a family member with an illness, your healthcare provider may order genetic testing to find the HTT gene.
Before passing the test, it is important to talk with a genetic consultant who can help you understand the possible test results.For example, if the test is positive, your consultant can explain what it means to you and (if you have children) the future of your child’s health.
There is no medicine of Huntington’s disease, but non-structural medications and therapies can be used to alleviate certain symptoms and improve the quality of human life.
The symptoms of involuntary movements can be treated XENAZINE
(tetrabenazine), the only medication,Approved by US food and medicinal medicines for Huntington’s disease.
, while xenazine is associated with possible side effects, such as:
anxiety (Akatisia )
parkinsonism (motion features,Visible in the disease Parkinson )
Other medications can also be used to treat cognitive, behavioral and emotional symptoms.For example, benzodiazepines can be used to treat anxiety and tasks in HD, while atypical antipsychotics, such as Zyprexa (Olanzapine), can be used to treat Korea, accompanied by psychosis, aggression or impulsiveness.
Rehabilitation methods of therapy
exercises through formal methods, as A> and professional therapy and informal, such as walking and daily, hotmut, help relieve symptoms.Seeing a nutritionist to avoid malnutrition, it is also useful, since he sees a speech and language therapist to swallow problems.
Additional treatment methods
Additional treatment methods that may be useful for people with Huntington’s disease include the Musical therapy, dance and play videogames.
Undoubtedly, there are many unique problems to live or care for someone with Huntington’s disease.The use of certain strategies can help you or your favorite person surf the way to follow.
Find the compatibility
Normally you have many problems if you or your favorite person were diagnosed or proven positive for the disease HuntingtonKnowing that there are many resources, and support networks are available, it can be useful since you learn what to expect and how to deal with.
An excellent resource is Huntington’s society of Huntington
in addition to educational tools, this organization coordinates support groups throughout the country, both on the Internet and personnel.This is not only for people with Huntington, but also for guardians, family members or people at risk.
Live all the best
The Havitled lifestyle can improve the quality of life, performance, dignity And the comfort man who live with Huntington’s disease.
Some of these healthy habits include:
Informal routine settings Use signals and indications, such as the phone alarm to point when the task (for example,Reception medication) It is necessary to complete
Attract a pleasant hobby,I like to listen to music or board games
Avoid alcohol and smoking
Administration of mental health symptoms
Compared with physical symptoms such as Khorora, psychiatric symptoms,Huntington is associated with depression and concern may be equal to no more complex and manage.
Rapid treatment of psychiatric symptoms is important and may include a combination of medications and psychotherapy.Unfortunately, suicide is common in people with Huntington.
If you have suicidal thoughts, contact LifeLeLine Theate
National Suicide Prevention at 1 -800-273-8255 With a prepared consultant.If you or beloved are nearby, call 911.
The forecast of Huntington’s disease is bad at this time. Average life expectancy after diagnosis is 10 to 20 years.
Word of the medications received
Huntington’s disease is an incurable and fatal state.Despite the complaint of symptoms, comfort, knowing that you (or your favorite person, if careful), you will still find joy and understanding that use support networks, spiritual growth or through your daily life approach.