Luca Sangiorgi

This study is creating a detailed registry to collect health information from people with Multiple Osteochondromas, a rare genetic condition causing bony growths. It aims to gather data on symptoms, treatments, genetics, and quality of life from up to 10,000 participants to bette…

This study is creating a large database to collect detailed health information from people with Ehlers-Danlos Syndrome (EDS). It aims to gather data on symptoms, treatments, surgeries, genetics, and quality of life from up to 3,000 participants. By linking all this information, r…

This study aims to create a detailed registry of information from people with rare bone diseases, primarily in Italy. Researchers will collect medical history, genetic data, and treatment details from up to 1,000 participants. The goal is to better understand how these diseases p…

This study is creating a detailed health registry for people with Osteogenesis Imperfecta (brittle bone disease). It aims to collect and link information from up to 5,000 patients in Italy about their symptoms, treatments, genetics, and quality of life over time. The goal is to b…

This study is creating a detailed registry to learn more about Ollier Disease and Maffucci Syndrome, two rare conditions that cause benign bone tumors. It will collect health information, family history, and treatment details from up to 400 participants in Italy. The goal is to u…