Huntington's
disease is an adult-onset, genetic brain disorder characterized by loss
of muscle control and advancing deterioration of the thought processes.
The early stages of Huntington's disease primarily affect the muscular
system. With progressive deterioration of the brain tissue, other organ
systems exhibit manifestations of the disease. The National Institute of
Neurological Disorders and Stroke states that more than 15,000 adults
in the United States are living with Huntington's disease as of 2010.
Musculoskeletal System
Huntington's
disease profoundly affects the musculoskeletal system due to loss of
brain cells, or neurons, that control the initiation, coordination and
fluidity of movement. The first symptoms of Huntington's disease
typically appear between the ages of 30 to 50, reports the University of
Utah Genetic Science Learning Center. Muscle twitching and lack of
coordination often herald the disease. Progressive loss of the neurons
that control movement leads to additional symptoms, including speaking
difficulties, clumsiness, random eye movements and involuntary jerking.
Lack
of coordination and involuntary jerking, or chorea, lead to an
increased risk for falls and broken bones. In the advanced stages of
Huntington's disease, loss of controlled muscular function leaves
patients incapable of performing the tasks of daily living, such as
feeding themselves, dressing, bathing and walking. People with
late-stage Huntington's disease are frequently bedridden and unable to
speak.
Digestive System
Huntington's
disease adversely affects the digestive system. Loss of muscle control
causes chewing and swallowing difficulties. The American
Speech-Language-Hearing Association notes that people with Huntington's
disease typically have difficulty holding food and liquids in the mouth,
initiating swallowing and clearing food from the mouth. Uncoordinated
activity of the esophagus, which transports food from the mouth to the
stomach, often leads to regurgitation of swallowed food. Eating
difficulties result in progressive weight loss, a hallmark symptom of
advanced Huntington's disease. A declining appetite may also contribute
to poor nutritional intake.
Loss
of muscle control usually leads to an inability to control the passage
of stool. Most people with advanced Huntington's disease have fecal
incontinence. Fecal contamination of the external opening for urine
passage may lead to urinary tract infection, especially among women.
Respiratory System
Swallowing
normally triggers a reflex muscular contraction of the epiglottis, a
piece of tissue in the throat that covers the opening to the airway to
prevent food from entering the lungs. The disordered swallowing
associated with Huntington's disease commonly interferes with the
coordinated closure of the airway, causing frequent episodes of choking
and contamination of the airway with ingested food and liquids. Food
contamination of the lungs frequently leads to pneumonia. The
Huntington's Outreach Project for Education at Stanford University
reports that pneumonia is the leading cause of death among people with
Huntington's disease.
Source Link: https://www.livestrong.com/article/188900-what-are-the-organ-systems-affected-by-huntingtons-disease/
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