Nijhuis, Wouter; Franken, Anton; Ayers, Kara; Damas, Chantal; Folkestad, Lars; Forlino, Antonella; Fraschini, Paolo; Hill, Claire; Janus, Guus; Kruse, Richard; Lande Wekre, Lena; Michiels, Lieve; Montpetit, Kathleen; Panzeri, Leonardo; Porquet-Bordes, Valerie; Rauch, Frank; Sakkers, Ralph; Salles, Jean Pierre; Semler, Oliver; Sun, Jony; To, Michael; Tosi, Laura; Yao, Yangyang; Yeung, Eric Hiu Kwong; Zhytnik, Lidiia; Zillikens, Maria Carola; Verhoef, Marjolein
(BioMed Central, 2021-03-20)
Background: Osteogenesis Imperfecta (OI) is a genetic disorder also known as ‘brittle bone disease’. The clinical manifestation of OI shows a wide variation. Therefore, care for patients with OI requires an interdisciplinary ...