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The Primary Cause Of Huntington’s Chorea

Huntington’s disease is a rare, hereditary neurodegenerative disorder that exerts a profound influence on an individual’s quality of life, manifesting in impairments of motor function, cognition, and mental health. Regrettably, there is currently no cure for this condition, but there are treatment and medication options for symptom management, such as prescription medications like haloperidol, tetrabenazine, amantadine, and Austedo which specifically helps with chorea. If you’re concerned about finances, such as Austedo XR hdchorea medication costs, be sure to look for discounts or purchase health insurance for coverage. Unlike many other conditions, the risk of developing Huntington’s does not rely on sex, ethnicity, lifestyle, nutritional choices, and so on. This disease causes symptoms such as uncontrollable movements (chorea), abnormal body postures, and issues with behavior, emotions, thinking, and personality. Here is the primary cause of Huntington’s chorea: 1.Inherited faulty gene Firstly, before symptoms even begin, Huntington’s can manifest in the body and not show up until a person’s 30s or 40s. As mentioned, Huntington’s is a hereditary disease—it is possible for sporadic Huntington’s to occur, but most often a diagnosis comes from an inherited faulty gene. When a parent has Huntington’s, each child has a 50% chance of inheriting the copy of chromosome 4 that carries the HD mutation—if a child does not inherit it, they will not develop the disease and they cannot pass it to future generations.