Tay sachs disease in adult

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Tay-Sachs is a disease of the central nervous system. It is a neurodegenerative disorder that most commonly affects infants. In infants, it is a progressive disease that is unfortunately always fatal.

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Most people with Tay-Sachs have the infantile form. In this form, the nerve damage usually begins while the baby is still in the womb. Symptoms usually appear when the child is 3 to 6 months old. The disease tends to get worse very quickly, and the child usually dies by age 4 or 5. Late-onset Tay-Sachs disease, which affects adults, is very rare.

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Unfortunately many healthcare providers are not aware of the rare adult forms of these diseases and dismiss the initial diagnosis due to the age of the patient. However, like all forms of Tay-Sachs, the LOTS form is only confirmed by a blood test to see the actual levels of Hexosaminidase A (Hex-A) they have.


The adult type of this genetic disease is not fatal like infantile and juvenile types The disease is named after Warren Tay, a British Ophthalmologist in when he described the characteristic cherry red spot and after Bernard Sachs, a neurologist from the United States.5/5(19). Tay-Sachs disease is broken down into the classic or infantile form, the juvenile form, and the adult or late-onset form. In individuals with infantile Tay-Sachs disease, symptoms typically first appear between three and five months of age.
Tay sachs disease in adult
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Jan 22, ยท Tay-Sachs disease is a rare, inherited neurodegenerative disease. People with Tay-Sachs disease do not have enough of an enzyme called beta-hexosaminidase A. The less enzyme a person has, the more severe the disease and the earlier that symptoms appear.

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