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Tools to help you identify, understand, and treat hypophosphatasia (HPP)

Webinars

Informative hypophosphatasia talks, case studies, and survey data

A webinar presented by Dr. Jill Simmons and Dr. Katherine Madson and hosted by Dr. Camille Bedrosian of Alexion Pharmaceuticals
A look of the impact of hypophosphatasia through a case study and survey data

Videos

Learn about hypophosphatasia mechanism of disease, critical care points, and diagnostics

Patient Testimonials

Patient and family experiences with hypophosphatasia

"The biggest struggle for me is the energy and keeping my pain at a place where I can still function."

"I first learned of hypophosphatasia when Abigail was diagnosed at 7 months old."

"I was born with it, struggled a lot through birth and my teen years."

"He gave me a blood test, and sure enough, my alkaline phosphatase was very low."

"We kept telling them . . . it’s not a nutrition issue, it’s something else."

"She looks like everything’s fine, when underneath there’s so many issues…"

Downloads

In-depth papers and print resources on diagnoses, critical care points, lessons learned, and analysis of hypophosphatasia

Hypophosphatasia websites

You're not alone in helping patients with hypophosphatasia. Explore further resources from other professionals and organizations treating hypophosphatasia.

Hypophosphatasie Deutschland e.V.

Hypophosphatasie Europe

Soft Bones: the US Hypophosphatasia Foundation

MAGIC Foundation

We are providing links to third-party websites solely as a convenience to you, because we believe those websites may provide useful content. We are not, by referring or linking to third-party websites, incorporating their contents into our own website. We do not endorse or guarantee, and we disclaim any responsibility for the content, products, or services offered on those websites, their performance or interaction with your computer, their security and privacy policies and practices, and any consequences that may result from visiting those websites.

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