If you or a loved one is experiencing any of the Multiple Endocrine Neoplasia syndromes symptoms, you are not alone. About half of people who have the disease have family members who have also been diagnosed with the disorder. While most cases of this disorder can be treated with targeted therapies, other treatment options may include surgery. Thankfully, there is an available treatment option for those who have experienced the symptoms of this condition.
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There are several types of multiple endocrine neoplasia. The most common type is called MEN1 and is caused by a genetic fault in the MEN1 gene on Chromosome 11. This gene is responsible for producing the protein menin. Most patients with the disorder have tumors in at least two endocrine glands, though they can form in other organs as well. The disease can be noncancerous or cancerous. It is important to note that some patients have no family history of the disease. It is possible for a person to acquire mutations in the MEN1 gene on their own.
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MEN1 is a type of multiple endocrine neoplasia that is caused by a mutation in the MEN1 gene. The MEN1 gene is located on Chromosome 11 and is responsible for producing the protein menin. Although this type of disease is caused by a defect in the gene, in some people the fault is not present. This causes a person to produce abnormally large glands that produce excess hormones. They can develop in more than one organ, and the changes often occur slowly over a period of time.
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MEN1 is inherited. It is caused by a mutation in the MEN1 gene. It can be passed from parent to child, but is not sex-linked. There is a 50% chance that a child will inherit the gene and MEN1 symptoms. Some patients do not have a family history of the disorder, and develop the mutation on their own. If you have a family history of this disease, you should seek treatment right away to prevent its progression.
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MEN2 can affect any part of the body. A person with MEN2 will likely experience hyperparathyroidism, a disease that can cause high blood pressure. The symptoms of this condition can vary from person to patient, and can be difficult to identify. However, if you are suffering from this disease, you should consult a doctor as soon as possible. Your medical professional will perform a diagnosis to rule out any other possible causes and diagnose the illness.
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Patients with this disease will typically have an increased risk of hyperparathyroidism, but they may also be at higher risk for hyperparathyroidism. Symptoms of MEN2 range from minor to severe, and may be difficult to diagnose. While the condition is not contagious, it can affect any member of the family. Because of the potential for complications, people with MEN1 should seek medical attention immediately.
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Symptoms of Multiple Endocrine Neoplasia syndromes can vary greatly from person to person. Most of the symptoms of MEN are the same in both types, but they can be slightly different in some cases. In order to understand which type of Multiple ENaplasia Syndromes you have, it's important to seek medical attention. A doctor will assess your symptoms and help you determine the best course of treatment.
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MEN2 is a rare tumor that affects the adrenal gland. It affects the body's metabolism and produces excessive hormones. Some patients have high blood pressure, heart palpitations, and excessive sweating. MEN2A is more aggressive than MEN2B, but the symptoms vary from person to person. Some symptoms of MEN2A are more noticeable in type 2B, and some are more subtle.
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There are several different types of Multiple Endocrine Neoplasia. The most common type is called type 1, which has three major subtypes: MEN1 and MEN2A. In both types, the tumors are in the same location and affect the same organs. Because of the genetic makeup of each type, the disease symptoms will vary from one individual to another. But MEN2 is more common in women than in men.
