{"id":49413,"date":"2024-07-21T10:00:51","date_gmt":"2024-07-21T04:30:51","guid":{"rendered":"https:\/\/gomedii.com\/blogs\/english\/?p=49413"},"modified":"2024-07-29T18:13:52","modified_gmt":"2024-07-29T12:43:52","slug":"how-much-tuberous-sclerosis-treatment-cost-in-india","status":"publish","type":"post","link":"https:\/\/gomedii.com\/blogs\/english\/treatments\/how-much-tuberous-sclerosis-treatment-cost-in-india\/","title":{"rendered":"How much Tuberous Sclerosis Treatment Cost in India?"},"content":{"rendered":"

Tuberous Sclerosis<\/b>, the rare genetic condition also known as Tuberous Sclerosis complex (TSC)<\/strong>, is the cause of tumors found throughout the body. These enlargements are not harmful but <\/span>Tuberous Sclerosis treatment cost in India may be high. However, benign tumors are abnormal growths of tissue and cells which are also known as non-cancerous tumors.<\/span><\/p>\n

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Early childhood or infancy is when most cases of Tuberous Sclerosis start. Sometimes the disease is misdiagnosed or not identified until adulthood because the signs and symptoms of Tuberous Sclerosis are so mild. Significant impairment can occasionally result from Tuberous Sclerosis.<\/span><\/p>\n

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It is impossible to monitor the progression of Tuberous Sclerosis over time, and there is no known treatment for the condition. There are techniques, nevertheless, to lessen symptoms.<\/span><\/p>\n

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One possible cause of Tuberous Sclerosis is a mutation in the TSC1 or TSC2 genes, which regulate tuberin and hamartin, respectively. Together, these genes control how cells divide, develop, and enlarge.<\/span><\/p>\n

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Symptoms of Tuberous Sclerosis<\/h1>\n

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Every instance of Tuberous Sclerosis presents with a unique set of symptoms which are as follows:<\/span><\/p>\n

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