The Clinical Picture of Patients Suffering from Hypophosphatasia—A Rare Metabolic Disease of Many Faces
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If you would like to make a donation to Soft Bones in honor of August, please click the button below! Donate Here My name is…
My HPP story started at a very young age. I was quite young and our bedroom was upstairs, and the bathroom was downstairs. I would…
My name is Cindy. I was diagnosed with Hypophosphatasia before I was 2yrs old. This was back in the early 1970’s. They didn’t know much…
In the spring of 2020, I was officially diagnosed with Hypophosphatasia through genetic testing. In retrospect, the signs and symptoms have been evident since my…
If you would like to make a donation to Soft Bones in honor of Ray, please click the button below! Donate Here If you were…
Mail Address (P.O Box)
The US Hypophosphatasia Foundation
141 Hawkins Place, #267
Boonton, NJ 07005, USA.
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Office Address (Location for meetings and events)
1719 NJ-10, Suite 315
Parsippany, NJ 07054
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