Tay Sachs Disease [SIMPLIFIED] - Cause, Symptoms, Diagnosis and Treatment | Nucleotides

Tay-Sachs disease is a rare autosomal recessive condition that results from a mutation in HEX-A gene on chromosome 15 that leads to GM2 ganglioside build up within lysosomes in the neurons of CNS resulting in progressive symptoms of CNS degeneration including visual problems, hypotonia and seizures.

Whats in this Video?

0:00 What is Tay-Sachs Disease?
2:11 What are the symptoms of Tay-Sachs Disease?
2:56 How is Tay-Sachs Disease diagnosed?
3:32 What is the treatment for Tay-Sachs Disease?
4:46 Quick summary

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