HPP News

HPP News

Read about HPP from other verified and trustworthy sources.

Behind the Mystery of Hypophosphatasia Featuring Deborah Fowler and Cindy Reasor

What is Hypophosphatasia? Symptoms, Causes, Diagnosis, Treatment and Prevention

2022 Recipient of hypophosphatsia Research Grant Announcement- Nan Hatch, DMD, PhD

2021 Recipient of hypophosphatsia Research Grant Announcement – Fatma F. Mohamed, PhD

2020 Recipient of hypophosphatsia Research Grant Announcement- Flavia Amadeu de Oliveira, PhD

2019 Recipient of hypophosphatasia Research Grant Announcement- Dana Gaddy, PhD & Dobrawa Napierala, PhD

2018 Recipient of hypophosphatsia Research Grant Announcement- Dr. Brian L. Foster, PhD

2017 Recipient of hypophosphatsia Research Grant Announcement- Dr. Kathryn Dahir

2016 Recipient of hypophosphatsia Research Grant Announcement- Brian L. Foster, PhD

2015 Recipient of hypophosphatsia Research Grant Announcement- Dr. Luke Mortensen of Athens, Georgia

Rarity

MS RDAC Sign-On letter

Aruvant Announces ARU-2801 Data Presentations at the American Society for Bone and Mineral Research (ASBMR) 2021 Annual Meeting

For Those Living With HPP and/or on Strensiq: Learn More About the COVID-19 Vaccines – September 2021

What Is Hypophosphatasia? An Overview of This Rare Genetic Disorder

The Emotional Aspects of Hypophosphatasia: A Guide for Families

Photographs reveal people behind rare illnesses

Study supports gene therapy as a promising treatment for soft bone disease

Mel Williams was diagnosed with Hypophosphatasia at 52 – despite living with symptoms for her whole life

COVID-19 Vaccine Statement- January 2021

Foundation Grantee Spotlight: Soft Bones

Parents of 9-Year-Old with Rare Genetic Condition Help Raise Awareness

Tampa teen creates app to connect people fighting rare diseases

The baby born with soft bones

Why ‘bubbly’ five-year-old Anna won’t be beaten by bone disease

City trials lead to first treatment for rare bone disease

Mum raises funds for one-month-old with rare condition

Rare bone disease robbing boy of childhood

Father, 26, has had FOUR hip replacements due to a rare disorder

Orphan Diseases Look For Parents With A Cure

Breakthrough drug gives girl born without bones a new chance at life

Hypophophatasia News and Research

Dentistry today newsletter Todays Dental News

The first spontaneous animal model of human hypophosphatasia uncovered

15,000 Spaniards may unknowingly have hypophosphatasia bone disease

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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