Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja Congenital radioulnar synostosis is a rare bone disorder that may be isolated or associated with other disorders and that is characterized by failure of segmentation of the radius and ulna during embryological development, causing limited rotational movements of the forearm, which may lead to difficulties with some activities of daily living. Disease data Klasyfikacja Morphological anomaly Synonimy Radioulnar fusion Zrost promieniowo-łokciowy Kod ORPHA 3269 Kod OMIM 179300 Kod ICD10 Q74.0 Kod ICD11 LB90.3 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl