Luca Sangiorgi

This study is building a registry of up to 400 people with Ollier disease or Maffucci syndrome. Researchers will collect medical history, genetic data, imaging, and quality-of-life information to better understand how these rare conditions progress and affect daily life. The goal…

This study is building a registry of people with rare bone diseases. Researchers will collect medical history, genetic data, and treatment details to better understand how these conditions progress. The goal is to improve future care and knowledge, not to test a new treatment. Cu…

This study is a registry that gathers medical, genetic, and quality-of-life information from people with osteogenesis imperfecta (brittle bone disease). It aims to better understand how the disease progresses and how genetics relate to symptoms. No treatments or interventions are…

This study is building a large registry of up to 10,000 people with multiple osteochondromas, a rare condition that causes benign bone tumors. Researchers will collect medical history, genetic data, imaging, and quality-of-life information to better understand how the disease pro…

This study is building a large database of medical and genetic information from up to 3,000 people with Ehlers-Danlos syndrome (EDS). The goal is to track how the disease progresses over time and find links between genes and symptoms. Participants' data will be collected from med…