Causes And 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 begins affecting the organs, it destroys the function of the multiple roles of the nervous system and the brain cells. The disease causes advanced deterioration and loss of brain cells, and contributes to a devastating loss of motor functions followed by advanced cognitive and intellectual impairment.

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".

At this stage, the individual is completely dependent for their care. A major concern during this time is choking. Also, involuntary movements can either be very severe or have stopped completely ("What Is Huntington's Disease," 2017). Although no longer able to speak, the individual is usually still able to understand language and even be able to recognize family and friends. Those with HD often die due to complications from the disease not actually the disease itself, such as choking and infection ("What Is Huntington's Disease," 2017).

Huntington’s Disease is a late-onset fatal genetic disorder that results in the gradual deterioration of nerve cells in the brain. Typical symptoms include involuntary movements, loss of muscle control, depression,

Huntington’s disease is a neurological (nervous system) condition caused by the inheritance of an altered gene. A neurological disorder is a disease that can affect the central and peripheral nervous systems. Huntington’s disease is an incurable genetic brain disorder. The disease is an autosomal dominant disease, meaning a child only needs to inherit the gene from one parent to develop Huntington’s. Nerve cells become damaged when someone holds the HTT gene that produces a protein called huntingtin, as too much of this protein damages cells, and causes various parts of the brain to gradually deteriorate. Huntington’s disease causes changes in the central area of the brain, the basal ganglia, which can affect movement, emotions, and mental

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 a very detrimental disease causing many changes to the body, including slowing down the nervous system until the body is unable to function. This disease affects 1 in every 10,000 people (Geyer), and takes away sufferers’ lives at around 65 years old (Revilla). This inherited disease has unbearable effects on the body and can change an ordinary life in only a few quick years after the first symptoms. There is no cure or treatment for this disease which makes it very hard to accept that such a condition has been placed in your life, but there are predictive tests that you can choose to have to address whether you may or may not have Huntington’s disease, this is a choice that many question but it is based on whether

Huntington Disease is a rare inherited Neurological illness. This illness is passed down from generation, but may not show up until you are an adult and is may no never show up. It often appears in more than one member if it occurs in a family. This a Genetic Condition. The change in the genetic information that is passed down is what causes Huntington's Disease. This illness causes involuntary movements, severe emotional disturbance. Huntington causes parts of the brain to break down and lose some natural functions and affects the Nervous system. The very first noticeable symptoms of this illness in changes in personality and muscle twitches. You would usually start to notice these symptoms around the age of 30 to 50. The men and women with

Huntington's disease is when the nerve cells in your brain start to deteriorate and your physical, as well as mental, state start to go down the drain. A government statistic states that “Huntington’s disease affects an estimated three to seven per hundred-thousand people.” (U.S. National Library of Medicine) Though rare, the effects of the disease are horrendous. The symptoms of this sickness can include muscle problems, difficulty of speech, trouble swallowing, problems staying focused, difficulty staying organized, lack of impulse control, feelings of irritability, sadness, apathy, fatigue, and loss of energy. The same women, Nora Guthrie, set her son on fire while he was napping on the sofa. Even though her son was just a little shaken, her family realized the effects Huntington’s disease had on Nora and how she couldn’t control herself. (Lawrence 10-11) This shows how severe the symptoms of Huntington’s disease can be. Not only are you just physically incapacitate, but you also

Huntington’s disease, named after George Huntington, was discovered in 1872. It is a neurological condition that is caused by an altered gene. This gene is passed from parent to child, but the disease cannot be seen until a later age. As the disease affects the brain by death of brain cells, the patient loses thinking. Also loss of physical and emotional functions such as walking, feeling pain, and lack of display of emotion. The symptoms start to appear when adults are around the age of 30 as well as up to 70. The most common symptom of Huntington’s is chorea. Chorea is where the body jerks, usually in the arms and legs. They may also experience difficulty speaking, swallowing, and focusing.

Huntington’s disease is a fatal genetic disorder which causes brain nerves to degenerate and die. The disease deteriorates a person’s physical and mental abilities at the age of 30 to 50. Most people who suffer from Huntington’s die before they are in their 50s. A child has 50% chance of inheriting Huntington’s if one of their parent suffers from Huntington’s disease. In early stages of Huntington’s disease, the patient will feel small coordination issues and irritable of depressed mood. In the middle stage of Huntington’s the coordination issues become more prominent and involuntary movements occur. It might be difficult to swallow or talk. Patients also experience trouble during problem solving. In the final stage of the disorder the patient

Huntington’s chorea, or more commonly known as Huntington’s disease (HD), is a neurodegenerative disorder that affects both men and women. Although previously thought to be a relatively rare disease, new research discoveries show that it’s actually more common than not; while the onset of symptoms typically occurs in a person’s 40s and 50s, research has also shown that individuals in their 70s, 80s and even 90s have enough repeats in the HTT gene to develop mild HD symptoms. (Samson, 2016) Through the selective degeneration of neurons and with the loss of neurons from the striatum and cerebral cortex, Huntington’s disease affects the nervous system by impacting movement, cognitive abilities, as well as neuropsychiatric symptoms. Unfortunately

Huntington's disease is a neurodegenerative hereditary condition which causes problems in muscle coordination, behavioral symptoms and leads mental deterioration (Hammond and Tatum 2010). Symptom varies among persons of same family. The most punctual side effects are frequently unpretentious issues with state of mind or insight.

Huntington’s Disease (HD) is a genetically inherited, progressive, autosomal dominant, fatal neurodegenerative disease that’s characterized by behavioral difficulties, decline of cognitive abilities, abnormal involuntary movements (chorea), and muscle spasms (dystonia) (1). These characteristics help diagnose patients with HD, but a genetic test can be done to prove that one has the disorder. The gene responsible is that which produces the huntingtin protein in chromosome 4; the defect causes extra repeats of the chemical code (2).