Tay Sachs Disease

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Volume: 50%
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About This Program

Tay-Sachs disease is a rare, inherited genetic disorder caused by a deficiency of the enzyme hexosaminidase A, which leads to the accumulation of fatty substances in the nervous system. It primarily affects infants, with symptoms typically appearing around six months of age, including developmental delays, loss of motor skills, and increased sensitivity to sounds. The disease is a type of GM2 gangliosidosis and is most commonly found among individuals of Ashkenazi Jewish descent, though it can occur in any ethnic group. This program includes frequencies that have been associated with Tay-Sachs disease in traditional Rife frequency literature. This entry is for informational purposes only, and users should consult a qualified healthcare provider for any health concerns.

Frequencies (10)

  • 200 Hz
  • 120 Hz
  • 27500 Hz
  • 47500 Hz
  • 96500 Hz
  • 275030 Hz
  • 534250 Hz
  • 691270 Hz
  • 753070 Hz
  • 927100 Hz

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