MEN1 and MEN2 are two of the most common types of Multiple Endocrine Neoplasia. Each of these diseases is caused by changes to a specific gene. MEN1 and MEN2 are hereditary conditions, which means that one or both parents must have an altered gene to pass it on to their children. While MEN1 is a common disease, the other forms can be inherited from either parent.
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The two most common types of MEN are type 1 and type 2. The first affects the pituitary gland and the other two affect the thyroid and parathyroid glands. In MEN1, the thyroid produces too much calcium, causing dangerously high blood pressure. In Type 2, only medullary thyroid cancer is found. The third type, MEN2B, is less common.
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MEN1 is an inherited disease that results in the growth of tumours in the pituitary gland, pancreas, parathyroid glands, and adrenals. Other symptoms of MEN1 include hyperparathyroidism, muscle pain, constipation, kidney stones, and thinning of bones. Although the symptoms of MEN are relatively common, it's important to seek medical attention right away if you suspect you might have MEN.
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Symptoms vary, but usually involve several different types of abnormalities in one gland. In type 1, the disease often involves the pituitary gland and the parathyroid gland, which release excessive amounts of calcium into the bloodstream. MEN1 is the most common type of the condition and is inherited from both parents. The disease can appear at any age. If the affected glands are affected, they may develop tumors on more than one organ at a time.
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There is no specific cure for MEN. Genetic testing can help identify the disease in family members of people with MEN1. Symptoms vary widely from person to patient and are based on the type of MEN. There is no known cure for MEN. In addition to genetic testing, doctors will often treat the affected glands as they appear. This treatment will depend on the type of MEN1 and MEN2 and their symptoms.
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While MEN1 and MEN2 are different in their symptoms, they share similar symptoms. For type 1, the affected glands usually have multiple endocrine neoplasia. In type 2, patients may have tumors in several organs. Some patients may also experience hyperparathyroidism. This condition may also result in a thyroid tumor. It is not known whether this disease will eventually lead to a death, although the disease will most likely cause life-threatening complications.
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MEN1 causes tumors in the parathyroid gland. In type 2, MEN1 patients may have abnormal hormone levels. A person with MEN1 may experience multiple endocrine neoplasia type 2 will have several of the signs and symptoms listed above. In severe cases, the tumors may affect other organs as well, such as the digestive tract, brain, and lungs.
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MEN1 is a genetically transmitted condition with several endocrine gland tumors in the body. The symptoms of MEN1 are similar to those of type 1, but in Type 2 patients, a RET gene mutation may be present in the mother's cells. It can also be present in a child's cell when the child is being formed. Some children with MEN2 will have an enlarged pancreas and an underdeveloped hypothalamus.
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The symptoms of MEN1 vary depending on the affected glands. The most common symptoms include hyperparathyroidism, constipation, and muscle pain. Some people with this disorder may also have changes in their digestive tract, including kidney stones. However, MEN1 symptoms are not limited to these two glands. For the most part, this disorder is not a life-threatening disease. In fact, if the condition is caught early enough, it can be cured.
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The symptoms of MEN1 depend on the specific types of MEN1 (a gene mutation) that a person has. MEN1 Type 2 occurs in both men and women. The symptoms of this disease may be different in both sexes. For a diagnosis of Multiple Endocrine Neoplasia, it is crucial to consult a doctor immediately. A specialist can make a decision based on the available information.
