Wilson Disease Essay example -- Health, Homeostatis

A forbearing nonplused with symptoms that suggested she expertness be schizophrenic. With many conditions mimicking schizophrenia, the doctor reviewed the notes from the family and noticed the patient had missed an essence doctor appointment. The physician, very aware an exam could confirm or confound a diagnosis, requested an eye examination be performed. Kayser-Fleischer rings were present in the cornea of her eyes. These rings are deposits of slob and sulfur granules and are greenish-gold in color. They are not always present however, when they are, they are a real identifier of Wilson sickness. (Holtz, 2006, pp.108-109) Therefore, the eye exam confirmed a diagnosis of Wilson disease for this patient. enchantment working in England during the early 1900s, Alexander Kinnear Wilson, an American neurologist, described the disease. (Schilsky & Brewer, 2009) As with many things, because he was the ace who originally described it, it is named after him. Wilson disease is also referred to as hepatolenticular degeneration. (Mayo Clinic, 2009).It is a genetic, chronic disease that stores up dissipation copper in the colored. Accumulation of excess copper begins at birth. (Childrens Hospital of Pittsburg, 2010) Copper is an essential trace metal vital to human being health, requiring a small, regular intake to maintain homeostatis. According to Copperinfo (2011), At least(prenominal) 20 enzymes contain copper and at least 10 of these admit copper to function. The brain, the skin, the heart and the immune system all need copper. Ingested copper is absorbed in the stomach and small intestine. From there, it enters the bloodstream, making its way to the liver. (Copperinfo, 2011) A healthy liver serves as a filter. Part of its functionality is metabolizing carbohydr... ...cinnati Childrens Hospital, 2009).A normal liver adequately filters and removes toxins from the body through the urine or bile. A lack of copper homeostatis in a diseased, damaged liver o bstructs this process. This excess accumulation of copper in the liver is Wilson disease. Inherited mutated genes, one from each parent, cause the disease. If only one mutated gene is passed on, then the soul is just a carrier and will never be diagnosed with Wilson disease. It is ordinary worldwide, including several different ethnic groups. It most often affects children and teens from ages 10 to 20 years old. Occasionally there are exceptions and we see diagnoses of Wilsons in children as young as three and adults over the age of 50. intervention is available that, if continued for a lifetime, will maintain copper homeostatis and the patient will live a good life.