Huntington's disease

of the more devastating mental disorders today is known as Huntington’s disease (Huntington’s chorea). Huntington’s largely affects people of European ancestry the most, an estimated three to seven out of every 100,000 of this decent suffer from it. Named after George Huntington who first characterized the effects of adult onset Huntington’s at the age of 22. In 1872, in the newspaper The Medical and Surgical Reporter, he described a disease that exhibited; loss of motor control, altered personality

much about Huntington’s disease. After reading this paper and the subsequent ones to come, you surely will. According to PudMedHealth.com, “Huntington’s disease is a disorder passed down through families in which nerve cells in certain parts of the brain waste away or degenerate.” This can lead to many different complications to a person’s health. In most cases, the disease’s symptoms develop later in life during a person’s mid thirties-forties. There are also instances where the disease becomes on-set

Huntington's Disease Background Huntington's disease is inherited as an autosomal dominant disease that gives rise to progressive, elective (localized) neural cell death associated with choleric movements (uncontrollable movements of the arms, legs, and face) and dementia. It is one of the more common inherited brain disorders. About 25,000 Americans have it and another 60,000 or so will carry the defective gene and will develop the disorder as they age. Physical deterioration occurs over a period

Huntington’s Disease Huntington’s disease also known as HD is a deadly inherited genetic disorder that causes the progressive breakdown of the nerve cells in the brain. Huntington’s disease deteriorates a person’s physical abilities such as eating or simply tying a shoe and it deteriorates a person’s mental abilities such as remembering simple addition during the mid adulthood lifespan. Within 10 to 20 years, a person with HD will lose his or her ability to eat, talk, and walk. The affected individual

Huntington’s disease is an inherited brain disorder that has a broad effect on a person’s physical and mental abilities. Unlike other passed down diseases, signs and symptoms of Huntington’s disease can start at any age but usually show between the age of thirty and forty. The onset of this disorder may even begin at the age of 20 or even before that and is known as the juvenile Huntington’s disease. Individuals with this disease can only live about 15 to 20 years after signs and symptoms appear

situation occurs when this gene becomes mutated. In this case, the individual will suffer from Huntington’s Chorea, a debilitating neurological disease which will not show its effects until mid-life.

Huntington’s disease is a degenerative neurological disorder affecting movement, cognition, and emotional state (Schoenstadt). There are two forms of Huntington’s disease (Sheth). The most common is adult-onset Huntington’s disease, with persons usually developing symptoms in their middle 30s and 40s (Sheth). There is an early onset form of Huntington’s disease, beginning in childhood or adolescence, and makes up a small percentage of the Huntington’s population (Sheth). Huntington’s disease is a

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

Huntington’s is a hereditary disease. A crucial part of the diagnosis process is to take a family history. The most efficient way to determine if the individual has this disease would be a DNA determination, showing a CAG repeat of at least 36 on the huntingtin gene that is located on chromosome 4. In most cases, the three main signs of this disease is present in the individuals. More studies are known to use biomarkers to determine the parameter’s as well. More studies are starting to focus on changes

Introduction 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 Clinical