About This Program
Sandhoff disease is a rare genetic disorder that affects the metabolism of certain lipids in the body, leading to severe neurological impairment. It is classified as a type of GM2 gangliosidosis and is caused by mutations in the HEXB gene, which result in a deficiency of the beta-hexosaminidase enzyme. This enzyme is critical for the breakdown of complex lipids; when it is deficient, toxic accumulation occurs in nerve cells, leading to progressive neurological decline. Symptoms typically manifest in infancy or early childhood and include developmental delays, muscle weakness, and sensory loss. This program includes frequencies that have been associated with Sandhoff disease in traditional Rife frequency literature. This entry serves informational purposes, and users are encouraged to consult a qualified healthcare provider for any health concerns.
Frequencies (10)
- 170 Hz
- 550 Hz
- 950 Hz
- 5150 Hz
- 13980 Hz
- 137500 Hz
- 362500 Hz
- 697500 Hz
- 775000 Hz
- 922530 Hz
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Run all 10 Sandhoff Disease frequencies at once
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