HPP News HPP News Read about HPP from other verified and trustworthy sources. Behind the Mystery of Hypophosphatasia Featuring Deborah Fowler and Cindy Reasor Watch Now What is Hypophosphatasia? Symptoms, Causes, Diagnosis, Treatment and Prevention Read Here 2022 Recipient of hypophosphatsia Research Grant Announcement- Nan Hatch, DMD, PhD Read Here 2021 Recipient of hypophosphatsia Research Grant Announcement – Fatma F. Mohamed, PhD Read Here 2020 Recipient of hypophosphatsia Research Grant Announcement- Flavia Amadeu de Oliveira, PhD Read Here 2019 Recipient of hypophosphatasia Research Grant Announcement- Dana Gaddy, PhD & Dobrawa Napierala, PhD Read Here 2018 Recipient of hypophosphatsia Research Grant Announcement- Dr. Brian L. Foster, PhD Read Here 2017 Recipient of hypophosphatsia Research Grant Announcement- Dr. Kathryn Dahir Read Here 2016 Recipient of hypophosphatsia Research Grant Announcement- Brian L. Foster, PhD Read Here 2015 Recipient of hypophosphatsia Research Grant Announcement- Dr. Luke Mortensen of Athens, Georgia Read Here Rarity Read Here MS RDAC Sign-On letter Read Here Aruvant Announces ARU-2801 Data Presentations at the American Society for Bone and Mineral Research (ASBMR) 2021 Annual Meeting Read Here For Those Living With HPP and/or on Strensiq: Learn More About the COVID-19 Vaccines – September 2021 Read Here What Is Hypophosphatasia? An Overview of This Rare Genetic Disorder Read Here The Emotional Aspects of Hypophosphatasia: A Guide for Families Read Here Photographs reveal people behind rare illnesses Read Here Study supports gene therapy as a promising treatment for soft bone disease Read Here Mel Williams was diagnosed with Hypophosphatasia at 52 – despite living with symptoms for her whole life Read Here COVID-19 Vaccine Statement- January 2021 Read Here Foundation Grantee Spotlight: Soft Bones Read Here Parents of 9-Year-Old with Rare Genetic Condition Help Raise Awareness Read Here Tampa teen creates app to connect people fighting rare diseases Read Here The baby born with soft bones Read Here Why ‘bubbly’ five-year-old Anna won’t be beaten by bone disease Read Here City trials lead to first treatment for rare bone disease Read Here Mum raises funds for one-month-old with rare condition Read Here Rare bone disease robbing boy of childhood Read Here Father, 26, has had FOUR hip replacements due to a rare disorder Read Here Orphan Diseases Look For Parents With A Cure Read Here Breakthrough drug gives girl born without bones a new chance at life Read Here Hypophophatasia News and Research Read Here Dentistry today newsletter Todays Dental News Read Here The first spontaneous animal model of human hypophosphatasia uncovered Read Here 15,000 Spaniards may unknowingly have hypophosphatasia bone disease Read Here
