Luca Sangiorgi

This study is creating a large registry to collect detailed health information from people with Ehlers-Danlos Syndrome (EDS). It aims to gather data on symptoms, treatments, genetics, and quality of life from up to 3,000 participants, primarily in Italy. The goal is to better und…

This study is creating a detailed registry to collect health information from people with Multiple Osteochondromas, a rare genetic condition that causes bony growths. It aims to gather data on symptoms, treatments, surgeries, genetics, and quality of life to better understand the…

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…

This study aims to create a detailed registry of information from people with rare bone diseases, known as skeletal dysplasias. It will collect past and ongoing health data, including medical history, genetic information, and treatment details, from up to 1000 participants in Ita…