Most Common Symptoms Of Huntington's Disease

Huntington's Disease is a genetic autosomal disorder which effects the brain. It affects about 1 in 20,000 individuals. The symptoms of the disease do not start to occur until after or around 40 years of age. With the onset of the disease the patient starts to gradually deteriorate intellectually, this deterioration also causes involuntary movements. Scientists have only recently found the section of the gene which causes Huntington's disease, and this is allowed them to devise pre-symptomatic tests. However, a cure for the disease is yet to be found.

Huntington’s disease may be irreversible but it can be treated with proper treatment may slow down the effects of the disease and medical attention. In children who have symptoms of Huntington’s disease, some of the symptoms would be a rapid deteriorating in school performance, lack of swift movements, behavior changes etc...

Huntington's Disease is a devastating and progressive neurological disorder that resu lts primarily from degeneration of nerve cells deep in the center of the brain. The condition was first described by George Huntington, a physician in New York, in 1872. Even then, the physician recognized the all-encompassing factors of the disorder when describing it as, "coming on gradually but surely, increasing by degrees, and often occupying years in its development until the hapless sufferer is but a quivering wreck of his former self".

Huntington’s Disease is a genetic disorder characterized by the arrival of symptoms late in life, usually in the 30s or 40s. It is an autosomal dominant disorder, which includes nerve cells breaking down in the brain. There are both movement and cognitive symptoms related to this disease. Some movement symptoms are unintentional jolting, delayed eye movements, and a compromised manner of walking. Some cognitive symptoms are trouble organizing responsibilities, a deficiency of cognizance of one’s own actions and capabilities, and a difficulty in understanding fresh material. There are also psychiatric disorders associated with Huntington’s disease: depression, obsessive compulsion disorder, and mania. Huntington’s disease results from a mutation

Huntington’s disease is a neurodegenerative disorder that slowly breaks down somatic tissues. This degeneration causes a mass amount of chorea, change in mental functioning, change in behavior, decreased memory, along with other serious psychological problems. Since the mechanism of the disease is still not fully understood, there is no cure for the disease, but there are several therapies and medications available. All of the medication and treatment available only help to manage symptoms; they are just stalling the progression of the symptoms but not the overall disease.

Huntington’s Disease is an inherited disease of the brain where the nerve cells break down over time. Huntington’s disease can also be called HD or Huntington’s Chorea, due to over 90% of patients having Chorea as well as HD. Chorea is an abnormal body movement disorder, which affects people with HD when it comes to muscle spasms, and involuntary movements. HD is a very rare disease, fewer than 200,000 cases in the U.S. per year. If an immediate family member has HD, you have a 1 in 2 (50%) chance of inheriting the disease. After the condition appears, patient usually lives for 15 to 18 years, HD is a guaranteed death. HD can cause cognitive amnesia, memory loss, behavioral issues (irritability, lack of restraint, etc.), psychological problems (delirium, depression, paranoia, etc.), anxiety, apathy, mood swings, and many more.

“The time from disease onset to death is often about 10 to 30 years. Juvenile onset usually results in death within 10 years” (Huntington's disease, 2014). The rate of progression varies from person to person. The disease itself will not kill you, but complications from the disease. Pneumonia is the top cause of death of HD at 51.1 percent (Liou, 2010). Heart attack, kidney failure, gastrointestinal disease, and suicide are also some of the top complications with Huntington’s

Huntington Disease is a progressive brain disorder which causes uncontrolled movements, loss of thinking ability, and emotional problems. There are two types of Huntington Disease, Adult-onset and Juvenile. Adult-onset is the most common form of Huntington Disease and those diagnosed live about fifteen to twenty years after beginning symptoms. The early signs and symptoms include depression, small involuntary movements, irritability, poor coordination, difficulty in making decisions, and difficulty retaining new information. As it progresses, the involuntary movements become more pronounced causing issue with walking, speaking, thinking, reasoning abilities, and personality changes (1).

Huntington 's disease is a dynamic, neurological disorder. Tragically, it doesn 't demonstrate manifestations until people have reached they’re 30 's or more. 'Children whose parent 's have this genetic disorder have a 50-50 ' ( ) possibility of acquiring the trait.

In the United States, approximately 30,000 Americans have Huntington’s disease. Huntington’s disease, also known as Huntington’s chorea, is an autosomal dominant disorder that causes selected neural cell death. With this disease comes concerns regarding what the disease is, its history, and it symptoms. In addition to those components, its stages, diagnoses, and treatments are of great importance as well.

Huntington’s disease (HD) is monogenic neurodegenerative disorder characterized by motor, cognitive and psychiatric abnormalities. It consists of two types: adult onset and juvenile onset. The most common form is adult onset in which a person’s symptoms usually occur between 35-44 years old with a mean survival time of 15-20 years after onset, while the less common form known as the juvenile form begins in adolescence with a mean survival time of 10-15 years after onset.1

Huntington’s disease (HD) is a fatal genetic neurodegenerative genetic disorder affecting the brain. It results in uncontrolled jerking movements (chorea), cognitive and behavioural changes. HD leads to incapacitation of the patient and ends fatal. However, death rarely results from HD itself. It is typically due to complications of HD. HD was originally called Huntington’s chorea, because of the involuntary movements that looked like jerky dancing. Chorea is the Greek word for dancing. The majority of HD patients start developing the disease around 30 to 40 or even later. If HD onsets before the age of 20, the condition is called juvenile Huntington’s disease. This form of HD has often expresses the symptoms different and progresses faster

Discovered in 1872 by George Huntington, Huntington’s disease, also known as Huntington’s cholera, is a genetic disease that causes selected nerve cells in the brain to die (Johns Hopkins). This leads to uncontrolled movements, emotion problems, and decreased cognition. Generally acting as an adult onset disease, Huntington’s disease is commonly seen to begin in one’s thirties and forties. Once the symptoms begin, the patient generally lives fifteen to twenty more years before succumbing to inevitable death.

Most people who are affected with Huntington’s disease have the same physical type of effects. They usually have very random and jerky motions that they cannot control. They also

Huntington’s Disease is a rare autosomal disease that first originated in northern Europe. It is a progressive degenerative disease that affects about every 5 in 100,000 people. The offspring of the parent who has suffered from this disease has a 50% chance of inheriting Huntington’s disease as well. Symptoms usually being around the age of 35-40 years of age. Huntington’s Disease symptoms begin gradually, but with detrimental effects. In the beginning stages of Huntington’s Disease symptoms include personality changes such as depression and a short temper, restlessness, and choreiform. Choreiform is involuntary moment that is rapid and repeated many times.