Ivemark Syndrome

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About This Program

Ivemark Syndrome is a rare genetic condition characterized by a range of anomalies, including congenital heart defects and splenic agenesis, where the spleen is absent or underdeveloped. It is often associated with other organ system irregularities and can have implications for the immune system due to the spleen's important role in filtering pathogens and managing blood cells. The syndrome is thought to arise from genetic mutations, and affected individuals may require specialized medical care to monitor and manage associated health issues. This program includes frequencies that have been associated with Ivemark Syndrome in traditional Rife frequency literature. This entry serves solely as informational; users should consult a qualified healthcare provider for any health concerns.

Frequencies (10)

  • 160 Hz
  • 490 Hz
  • 620 Hz
  • 850 Hz
  • 7500 Hz
  • 162500 Hz
  • 281200 Hz
  • 492520 Hz
  • 675620 Hz
  • 825230 Hz

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