Searching for Tay Sachs Disease Life Expectancy And Support information? Find all needed info by using official links provided below.
https://rarediseases.info.nih.gov/diseases/7737/disease
Jan 22, 2018 · 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. There are 3 forms of Tay-Sachs disease, distinguished by the general age of onset:
https://www.healthline.com/health/tay-sachs-disease
Life expectancy varies with this form of the disease, and some people have a normal lifespan. Adult Tay-Sachs is the mildest form. Symptoms appear during adolescence or adulthood.
https://www.thinkgenetic.com/diseases/tay-sachs-disease/living-with/59265
What is the average life expectancy for someone with Tay-Sachs disease? The classic, infantile form of Tay-Sachs is a progressive disorder that often cause life-threating complications early in life. Most children pass away by the age of 4 or 5.
https://en.wikipedia.org/wiki/Tay%E2%80%93Sachs_disease
Tay–Sachs disease is a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord. The most common type, known as infantile Tay–Sachs disease, becomes apparent around three to six months of age with the baby losing the ability to turn over, sit, or crawl.Specialty: Medical genetics
https://www.thinkgenetic.com/diseases/tay-sachs-disease/organizations/42441
There are several support groups or organizations for Tay-Sachs disease that provide support, information, advice, referrals to physicians and medical centers, and up …
https://www.healthtap.com/user_questions/1564875-what-is-the-life-expectancy-of-someone-with-tay-sachs-disease
Tay Sachs disease is an autosomal recessive, neurodegenerative disease cause by excessive storage of Gm2 ganglioside withinn cell lysomes. Normal motor function first few months of life following by progressive weakness , starting at 2 to 6 months of age.
https://www.ntsad.org/index.php/find-support
Support for Families If your family is affected by a rare genetic disorder, you are not alone. NTSAD is here to help with resources that can help from the day of diagnosis through day-to-day care, tough end-of-life decisions and beyond.
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