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Recommended: Wilson's disease
What is Wilson‘s diseases? Wilson’s disease also known as a term called hepatolenticular is basically a genetic disorder and causes copper to start accumulate in the liver, brain and other vital organs. This accumulation then causes various troubles and problems related to the organs. Copper is an essential metal for our body and it plays a key role in the development of healthy nerves, bones, and collagen.
As we said that Wilson’s disease is a genetic disorder which mean it can be pass down from generations to generations. The main reason for this will be genetic mutation. For example, if you have received one gene then you won’t be affected from the disease rather you’ll become a carrier, which means you can pass this on to the next generation. Due to this mutation, the protein that helps in shifting excessive copper to the liver came to a problem. The picture below show how the mutation was passing down.
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We can easily receive copper from the foods we eat for example seafood like oyster. For normal scenarios, people usually take more copper than needed. The liver then will take the required amount of copper to perform the daily task and will help to releases the excessive ones out of the body. But, those who’re suffering from Wilson’s disease could not get rid of the excessive copper. The copper will then be deposited in the liver and later on cause damage to your organ like liver failure. With time, these excessive copper may start to leave the liver starts building up in other vital organs of the body; mostly eyes cornea, brains and kidneys which will lead to possible to life threatening level. Left untr...
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...th urine and sweat. The faecal excretion is in the greatest part due to the passage of unabsorbed zinc but it is also due to endogenous intestinal secretion.
Other possible drug interaction
The absorption of zinc may be reduced by iron and calcium supplements, tetracycline and
Phosphorus-containing compounds, while zinc may reduce the absorption of iron, tetracycline, fluoroquinolones.
Reaction mechanism of Zinc Acetate
Zinc works by increasing the levels of metallothionein in the intestinal cells, which reduces dietary copper uptake. Furthermore, it also reduces the reabsorption of endogenous copper, this facilitating its excretion and preventing copper from accumulating in the body.
From the table above, we can see by increasing the metallothionein which is in short MT helps to reduce the copper as the excess copper was being “trap “on the metallothionein.
Wilson had some important roles in World War I that took a tole on his health. Just the fact of being a president is enough pressure. What stands out most after much research is the fact of how much he wanted peace. One would not underestimate by saying he spent his life by trying to have world peace. He was a remarkable president and benefited our nation tremendously by his works.
Also evident are molluscoid pseudotumors (fleshy lesions associated with scars) frequently found over pressure points (e.g. elbows) and subcutaneous spheroids, which are commonly mobile and palpable on the forearms and shins. Complications of joint hypermobility include sprains, dislocation are common in the shoulder, patella and temporomandibular joints Muscle hypotonia and slower gross motor development also can occur It is inherited in an autosomal dominant manner (Clarke, D., Skrocki-Czerpak, K., Neumann-Potash, L.). In the Hypermobile type of EDS, the joints of the body experience Hypermobility, which is the dominant clinical manifestation. General joint hypermobility affects large (elbows, knees) and small (fingers and toes) joints. Skin is hyperextensible, smooth/velvety, and bruising occurs easily as well.
...ll understood simply because of the numerous genetic and environmental factors possible in causing any part of PDB, either by over stimulating osteoclast precursors, genetic mutations, producing transduction pathways that would otherwise not be present or even signals misfiring or over active parathyroid gland. Much more isolated research is necessary before this disease can be fully understood.
... (CNS) may also indicate another copper binding function for PrP. In blood and blood plasma, amino acids are mainly what copper binds to, yet the chief component which it actively binds to is Serum Albumin, which readily takes up 1 copper at its N terminal. The cerebrospinal fluid however, contains more amino acids and lacks a high quantity of serum albumin, and othe copper binding constituents normally found in blood. Thus it is hypothesised that PrP plays a role similar to albumin, by helping maintain copper homeostasis. Several studies have also shown that PrP opposes apoptosis reactions in some cells, by protecting the cells from the signals which would usually cause apoptosis to occur. Mutagenesis experiments have shown the PrP octarepeat domain is required to protect against Doppel-protein toxicity, which when usually expressed, would bring about cell death.
In 1980, the first reported case of Angelman disease was reported in America. As more and more children were being diagnosed with Angelmans disease, a professor from the University of Florida, Dr. Charles Williams, started researching the disease. Years went by with no progress, but then in 1987 Dr. Williams discovered that a code was missing from chromosome 15. This new information was a breakthrough, but it would still until 1997 to figure out that the UBE3A gene on chromosome 15 was mutilated or missing in patients diagnosed with Angelman disease. Since 1997 doctors and scientists have been able to find that Angelman disease is a neuro-genetic disorder which means that Angelman disease is very complex and attacks the nervous system. They have also been able to determine that the disease is rarely inherited and that the mutilation of the UBE3A gene occurs during sperm and egg formation.
Parkinson disease (PD), also referred to as Parkinson’s disease and paralysis agitans, is a progressive neurodegenerative disease that is the third most common neurologic disorder of older adults. It is a debilitating disease affecting motor ability and is characterized by four cardinal symptoms: tremor rigidity, bradykinesia or kinesis (slow movement/no movement), and postural instability. Most people have primary, or idiopathic, disease. A few patients have secondary parkinsonian symptoms from conditions such as brain tumors and certain anti-psychotic drugs.
Parkinson's is an idiopathic, multifactorial neurodegenerative disease that attacks neurotransmitters in the brain called dopamine. Dopamine is concentrated in a specific area of the brain called the substantia nigra. The neurotransmitter dopamine is a chemical that regulates muscle movement and emotion. Dopamine is responsible for relaying messages between the substantia nigra and other parts of the brain to control body movement. The death of these neurotransmitters affects the central nervous system. The most common symptoms are movement related, including shaking, rigidity, slowness of movement and difficulty with posture. Behavioral problems may arise as the disease progresses. Due to the loss of dopamine, Parkinson's patients will often experience depression and some compulsive behavior. In advanced stages of the disease dementia will sometimes occur. The implications of the disease on the anatomy and physiology of the respiratory and phonatory systems significantly control speech.
During digestion, the body breaks down food into smaller molecules that could then be used by the body’s cells and tissues in order to perform functions. This starts off in the mouth with the physical movements of chewing and the chemical breakdown by saliva. Enzymes in the stomach break food down further after traveling from the mouth through the esophagus. The food from here then moves into the small intestine, where pancreatic juices and enzymes dissolve proteins, carbohydrates, and fibers, and bile from the liver breaks down fats into these small molecules. Any portion of the fibers or food that were unable to be broken down are passed from the small intestine to the large intestine, which is where the digestive tract transitions into the excretory tract, then the colon and out of the rectum. Any liquids that have been stripped of their nutrients by the body proceed from the stomach to the kidneys. In the kidneys, sodium ions (Na+), uric acid, and urea are exchanged with water, which moves urinary bladder and is excreted through the
PD is known to be idiopathic, however, many studies have found that a combination of genetic and environmental factors are associated with the development of PD. Environmental risk factors include the use of pesticides, living in a rural environment, consumption of well water, and proximity to industrial plants or quarries. The genetic causes also have been studied and it was found that a genetic cause for the development of PD accounts for 5% of all cases (Hauser et al. 2010). Medications that block dopamine receptors also are considered to be a cause for the development of Parkinson disease. Int...
Iron is an essential part of a healthy diet. Iron compounds are employed for medicinal purposes in the treatment of anemia, when the amount of hemoglobin or the number of red blood corpuscles in the blood is lowered.
The human body needs potassium to function. The body may become short of potassium in many situations. Excessive physical activity, severe cases of stress, drinking of alcohol or coffee all consume the potassium in the body leaving the person with a deficiency of the mineral. As a result of this deficiency severe fatigues, muscle weakness, nervous disorders, cardiac arrest, and poor reflexes can occur. Too much potassium in the body may result in dehydration. The kidneys can retain or get rid of too much potassium. Either extreme is dangerous for the body.
Lead is considered to be a toxic heavy metal. It occurs naturally in the Earth’s crust. However, it tends to combine with other elements to form lead compounds. (Registry, 2011). Moreover, it has no known function in the body and with excess accumulation, either acute or chronic, will cause a wide array of metabolic dysfunctions by interfering with normal metabolic functions (Analytical Research Laboratories, 2012). From a historical standpoint, most human beings if not all have accumulated some lead in their bodies over the course of their daily lives. In extreme cases, that is, when there is too much lead in the body it is known to cause lead poisoning. In order to fully understand this phenomenon, one must first acknowledge; how lead enters the body, how it is distributed, and how and if it is eliminated.
...he Buttermilk White bread. The food makes its way to the transverse colon and extra nutrients are released form the cellulose of the undigested particles. It continues on to the descending colon. There I start to manufacture vitamin K and other B-complex vitamins. Those are then absorbed into my large intestine.
Once the alloy has been quenched in this condition it is now stronger because all of the 4% of Copper has been dissolved into the solution and ductile because the brittle crystals of the Cu〖Al〗_2 compound are now absent.
Most of the molybdenum content of food consumed is absorbed in the intestines and exits the body through the urine.