Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, genetic dysostosis malformation syndrome characterized by skeletal dysplasia (rabbit ear-shaped iliac alae, delayed bone age, abnormalities of the vertebral bodies and schisis of the vertebral arches), seizures, short stature, cerebral atrophy and moderate to severe intellectual disability. Additional variable manifestations include corneal and retinal abnormalities, cataract, prognathism, dental malocclusion, brachydactyly, clinodactily, slight generalized hypotonia and hyper extensible joints. Disease data Classification Malformation syndrome Synonyms Gurrieri-Sammito-Bellussi syndrome Zespół Gurrieri, Sammito i Bellussi ORPHA code 1858 OMIM code 601187 ICD10 code Q87.5 ICD11 code LD24.8Y *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