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 is a fatal genetic disorder that causes the progressive breakdown of
This paper discusses one of the most well known neurodegenerative diseases named Huntington’s. Recent statistical records showed that the disease is widely spread around the world. Scientists have conducted many researches in order to study the mode of inheritance of the disease as well as to find a possible cure for it. They discovered that the disease is genetically inherited from one generation to another. The aim of this scientific paper is to provide information about this genetic disorder including
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
family and settling down. Huntington’s Disease quickly takes all these dreams and ambitions away, along with control of ones body and mind. The symptoms of Huntington’s, such as involuntary muscle jerks or twitches, had been seen throughout history for many years before being first recognized as an inherited disease in 1872 by Dr. George Huntington (“Hope Through Research). “The hereditary
Huntington’s disease INTRODUCTION & AIM The aim of this project is to discuss the various components that shape Huntington’s disease. The efficiency of this paper will depend heavily on a brief but, comprehensive examination of past and future research that may offer plausible suggestions and explanations to the following four subtopics; the history of Huntington’s disease, anticipation and genetic markers of Huntington’s disease, symptoms and treatment of Huntington’s disease and finally living
with Huntington’s disease through human genome and family research. Diagnostic and presymptomatic testing is available by discovering a gene mutation for Huntington Disease (HD) and prepares persons who are at risk for Huntington Disease (HD) to ask for genetic testing. A multi-visit protocol is enacted when HD genetic testing is offered through HD testing centers, followed by education and counseling for those requesting to have HD gene testing. I will use this paper to define Huntington’s disease
Huntington’s disease affects 30,000 Americans and has 200,000 more Americans at risk to contract the disease. Huntington’s is now one of the most common brain disorders to be inherited. This paper will discuss and educate about the disease, pathology, signs and symptoms, etiology, prevalence, diagnostic studies, treatments, and the prognosis of Huntington’s disease. Huntington’s disease (or Huntington’s chorea) is a hereditary degenerative disease that affects the cerebral cortex and basal ganglia
Huntington disease is a genetic disorder that has affect many people. The Huntington disease is commonly known as Huntington Chorea (Genetics Home Reference ). The disease was first recognized in 1872 by George Huntington (Phillips). George Huntington wrote a paper called On Chorea and “chorea” is Latin and Greek for chorus or a group of dances (Phillips). In the Middle Ages this term was given to many “dancing disorders” (Phillips). People with chorea basically had involuntary muscle jerking and
unsuccessful trials to find a cure for diseases and disorders such as Alzheimer’s disease, Huntington’s disease, and/or Parkinson’s disease, it seems like scientific research has provided us with a hope for these diseases. This essay will address the issue of controversial research in stem cells. This technology offers hope to millions who are victims of a multitude of diseases and disorders. It can be used to regrow limbs, create organs, attack genetic diseases, treat malfunctioning bladders, etc.
This web page is helpful in identifying the cause of the Agammaglobulinemia disorder. Bittles, A. H., & Black, M. L. (2010). Consanguinity, human evolution, and complex diseases. Proceedings of the National Academy of Sciences, 107(suppl 1), 1779–1786. http://doi.org/10.1073/pnas.0906079106 Bittles is an Adjunct Professor and Research Leader at Murdoch University in Australia and is the author of the book “Consanguinity in Context”. M.L Black is employed at the Centre for Human Genetics at Edith Cowan