Dental Concerns in Patients with Rare Bone Disorders (OIF)

This recording and others are available on the OIF website at www.oif.org/echo
This recording and others are available on the OIF website at www.oif.org/echo
This recording and others are available on the OIF website at www.oif.org/echo
I was 22 years old when you were born and had a kindergartner, your brother, as well. I knew something was going on with you,…
Hi, we are twin sisters Amy and Suzanne, we have been dealing with symptoms of HPP for a lifetime. Our diagnosis seemed as though it…
Hello, My name is Morgan Salomon, and I am 16 years old, and I’d like to tell you a little bit about me and my…
Hello everyone, my name is Sharon T., and my husband Dave has hypophosphatasia (HPP). He and our family have paid a price in our HPP…
The US Hypophosphatasia Foundation
141 Hawkins Place, #267
Boonton, NJ 07005, USA.
Organization
Programs
Community
Responses