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Hypophosphatasia (HPP) resources for you

Knowing all you can about HPP is the first step to living every day with HPP. Sign up, stay connected, and see more! When updates are available, you will receive

  • The latest news on HPP
  • Information about upcoming webinars and live events
  • Real-world patient stories
  • Tips, tools, and resources for living every day with HPP

HPP resources for your doctor

Because HPP is a rare disease, your doctor may not know a lot about it. We can share educational information about HPP with your doctor.