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Published byMaximillian Fowler Modified over 9 years ago
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BY: Zach Kimmel
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Tay-Sachs disease Tay-Sachs disease is a genetic disorder that is fatal in most occurrences.
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TSD GM2 Hexosaminidase Sphingolipidosis TSD GM2 Hexosaminidase Sphingolipidosis
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Warren Tay
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Above is the strand of genes were the mutation occurs.
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Symptoms/ How the disease is passed on There is a distinct red spot in the eye of a patient with Tay-Sachs Disease. There is a distinct red spot in the eye of a patient with Tay-Sachs Disease.
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Types of Tay-Sachs
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Infantile TSD
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Juvenile TSD Extremely rare, Juvenile Tay-Sachs disease usually occurs in children between 2 and 10 years of age. They develop, speech difficulties swallowing difficulties, and unsteadiness. Patients with Juvenile TSD usually die between 5–15 years.
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It occurs in patients in their 20s and early 30s it is frequently misdiagnosed, and is usually non-fatal. Patients frequently become full-time wheelchair users in adulthood, but many live full adult lives. Psychiatric symptoms and seizures can be controlled with medications. This form of TSD is very, very rare.
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Prevention/Cure
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Works Cited http://en.wikipedia.org/wiki/Tay-Sachs http://organizedwisdom.com/Adult_Onset_Tay- Sachs_Disease http://www.ninds.nih.gov/disorders/taysachs/taysac hs.htm http://kidshealth.org/parent/medical/genetic/tay_sa chs.html http://en.wikipedia.org/wiki/Tay-Sachs http://organizedwisdom.com/Adult_Onset_Tay- Sachs_Disease http://www.ninds.nih.gov/disorders/taysachs/taysac hs.htm http://kidshealth.org/parent/medical/genetic/tay_sa chs.html
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