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What is Huntington's disease and is it deadly?
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What is Huntington's disease and is it deadly?

3 months ago
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Huntington or HD is a rare disease that is usually inherited from parents ... Symptoms of the disease may appear at any age, but often appear in the 1980s or 5.. If the disease occurs before the age of 6, it is called a teenager Huntington .... However, they cannot prevent the dementia of the physical, mental and behavioral reason caused by the disease.. What is the Huntington Disease List? What are the symptoms of Huntington? .. The cause of Huntington's disease in men and women The diagnosis of Huntington Huntington's Huntington Disease in Iran and the world is prescribed medications for the disease?. Huntington is an inheritance disease that causes brain cells to gradually disappear and eliminate. This affects parts of the brain that control voluntary movement and memory.. Common symptoms include uncontrollable movements and change of thinking, behavior and personality ... These symptoms exacerbate over time ... What is Huntington's symptoms? .. Huntington's disease usually causes motor disorders ... It also causes problems in mental health and cognitive abilities such as thinking and planning ... These conditions can have a wide range of symptoms .... Early symptoms vary from person to person and change during progression of the disease .... Motor disorders of motor disorders associated with the disease may cause uncontrollable movements, called Cria Huntington .... Caria contains involuntary movements that affect all muscles of the body, especially hands, feet, face and tongue. This disorder can also affect the ability to perform voluntary movements.. Symptoms include: involuntary movements of stiff or abnormal eye muscles ... Walking problems or maintaining body balance and decaying body disruption or swallowing people with HD may have difficulty controlling their voluntary movements.. This affects one's ability to work, perform daily activities, communicate and maintain personal independence .... HD leads to motor and cognitive disorders and increases the risk of mental health problems ... Cognitive disorders of the disease often cause problems in cognitive skills and lead to the following symptoms: Problem in organizing, prioritizing or focusing on non -flexibility or repeating obsessive -compulsive thoughts, behavior or ignorance of their behaviors and abilities to reduce information or learning speed .... Depression is the most common mental disorders associated with the disease and is caused by brain damage and function .... Symptoms of depression may include: Irritability, sadness, or indifference to sleep disorder sleep disorder, feeling fatigue and decreased energy or suicide ... Other common mental disorders include obsessive-compulsive disorder: The condition in which the person is disturbed and repeated .... Mania: Conditions that are associated with mood change, excessive activity, provocative behaviors and high self -esteem ... Bipolar Disorder: Conditions that include periodic periods of depression and mania .... In addition, people with Huntington may lose weight, especially as the disease progresses ... Online counseling with the best neurologists starts and improves Huntington's symptoms in children and adolescents in adolescents and children in adults.. Early symptoms include behavioral changes, including concentration problems, sudden decline in academic functioning, and behavioral problems such as aggression, such as stiffness and muscle contraction, which cause walking (especially in young children), vibrations or unnecessary diseases and unnecessary diseases, which means that it gets worse over time .... The stages of progression of the disease are: The initial stage: mild symptoms ... The mood may change and the patient may have difficulty thinking about complex issues .... It may also have uncontrollable small movements, but it is still able to continue its daily activities .... Middle Stage: It makes the physical and mental changes to work, driving and handling homework .... The patient may have trouble swallowing food, making it challenging and eating. It also disrupts one's balance and increases the risk of falling ... However, the patient can still take care of himself and bath and clothing alone ... Final stage: It is very difficult to do everyday tasks without the help of others .... Most people at this stage cannot get out of bed without help.. Under these conditions, especially for eating, bathing and monitoring health care is needed .... HD is a progressive disease that gradually worsens and affects one's quality of life.. Is Huntington's disease deadly? This disease is not fatal .... But over time, it makes everyday activities more difficult and may have side effects.. The rate of progression of the disease varies in people .... Usually the duration between the first symptoms and the death of about 2 to 5 years.. However, if the disease occurs at an early age, the patient dies within 2 to 5 years after the onset of symptoms .... HD depression can increase the risk of suicide .... Other factors that lead to the killing of these patients include: pneumonia (pneumonia) or other infections. Liability caused by reducing more complications related to swallowing disorder: What is Parkinson's? .. The cause of Huntington's disease in men and women is due to the change of a single gene inherited from parents .... Given that Huntington's disease is dominant or recessive, it follows a dominant autosomal inheritance pattern. This means that only one copy of abnormal genes is enough to obtain it .... People with one of their parents with HD are at risk for the disease .... Huntington's doctor's diagnosis diagnoses Huntington's disease through physical examination .... In this study, the physician assesses the problems of balance and coordination and seeks the symptoms that affect the movements .... In addition, he questions about the family history of the disease in close relatives. To reject other diseases that have similar symptoms, your doctor may prescribe the following tests: Blood testing of genetic testing of imaging tests such as MRI and CT Scan (CT SCAN) Treatment of Huntington Disease Treatment in Iran and the World is the purpose of treatment.. Because there is currently no way to stop, slow down or prevent symptoms .... Since HD affects physical and mental health, the patient may require a variety of therapies, including: Physiotherapy or occupational therapy therapy occupational therapy, there is no way to prevent HD progress.. But with existing treatments, quality of life can improve ... What medications are prescribed for this disease? Your doctor will prescribe different medications to manage symptoms .... The most common drugs for Huntington Korea are as follows: Halperidol tetalbenazine is also used to control mental symptoms: antidepressants such as fluoxetine and sertraline are anti -psychiatric drugs such as micropride and uranprobpin. For example, physiotherapy can cause muscle pain and medications can lead to fatigue or blood pressure.. Before starting treatment, your doctor will explain possible complications so that the patient can consciously decide on his or her health .... If you have Huntington's disease, you can improve your quality of life: Take care of yourself in person: Exercise regularly .... Research shows that exercise is helpful to improve your overall condition .... Be healthy .... Doctor may recommend changes in your diet .... Because irresponsible movements can burn up to 6,000 calories a day ... Drink enough water ... Increase the dehydration disorder ... Consult your doctor about hydrating the body .... Find a support group ... Ask your doctor how to communicate with other people with the disease ... Research on Care Services .... You will need a high level of care at some point in the disease ... determine a reliable consultant .. With the progress of the disease, you have to hand over your financial and personal decisions to a reliable person .... This is an important and difficult decision ... so it is better to make these symptoms worse .... Learn more: SMA Disease Ways to Prevent HD Huntington in their families may worry about transmitting the disease to their children.. In such circumstances, laboratory fertilization is recommended using sperm or eggs and genetic detection before transplantation (PGD).. In PGD, the eggs are taken from the mother's ovary and fertilized in the lab with the father's sperm .... The fetus is then tested for the presence of the Huntington gene to be in the uterus only the fetus that lacks this gene.. If you have a history of HD in your family, ask your doctor how to prevent the transmission of the disease to the next generation .... Huntington's last word over time reduces the ability to take care of the person.. Hearing the news that you or one of your loved ones have the disease can be very difficult ... However, with the progress of years of symptoms, you will have enough time to plan and prepare for long -term care .... You need to make important decisions about your health.. But you don't have to rush for these decisions ... because they can have a huge impact on your future .... If you need guidance on Huntington's disease and ways to control it, you can apply online for an online neuroscientist.. Also, the treatment of the company allows you to get an appointment from your specialist to see your neurological physician through an internet appointment system ... What are the common Huntington's disorder questions?. Huntington is a genetic disease that affects brain cells and worsens over time .... Symptoms of this disease usually appear in 5 and 8 lives ... Does Huntington treat?. There is no way to prevent the progression of the disease .... That's why doctors are trying to make the patient easier with existing strategies and improve the quality of life. Can Huntington be treated with stem cells? .. Stem cell -based treatments are in the research phase and have not yet been approved for extensive use .... Sources: Mayoclinic, My.ClevelandClinic Top Doctors: Dr. Maryam Soleimani | Doctor .. Javad Ameli Dr. ... Reza Sanjari Dr. ... shahab kamali ardakani dr ... behrouz sadeghi hariri Dr. ... Betul Dadkhah Dr. ... Dr. Hassan Mohammad ... Dr. Mohammad Samadi Doctor .. Nasser Mehraban Is this article useful to you? ... an average of 5.5 points .... The number of votes 1 is not yet registered {"Context": "http://schema.org", "Type": "CreativeWorkSeries", "Aggregateting": "" Type ":" Type ": Aggregateing", "Bestrating": "1": "RatingValue": "" "" "" "5" 5 "" 5 ".. "https://www.darmankade.com/blog/wp-content/uploads/2025/03/1-10.webp", "What is Huntington's disease and is it a disease?" Is it? .. ”}
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