Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja 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 Klasyfikacja Malformation syndrome Synonimy Gurrieri-Sammito-Bellussi syndrome Zespół Gurrieri, Sammito i Bellussi Kod ORPHA 1858 Kod OMIM 601187 Kod ICD10 Q87.5 Kod ICD11 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