Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition An extremely rare form of bone dysplasia characterized by the features of osteogenesis imperfecta such as bone fragility associated with multiple fractures, bone deformities (metaphyseal irregularities and bowing of the long bones) and blue sclera, in association with growth failure, craniosynostosis, hydrocephalus, ocular proptosis, and distinctive facial features (e.g. frontal bossing, midface hypoplasia, and micrognathia). Disease data Classification Malformation syndrome Synonyms Bone fragility-craniosynostosis-proptosis-hydrocephalus syndrome Kruchość kości - kraniosynostoza - proptoza - wodogłowie ORPHA code 2050 OMIM code 616294 ICD10 code Q78.0 ICD11 code LD24.KY *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