retinal disorder developmental disability osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome https://rarediseases.info.nih.gov/diseases/587/al-gazali-sabrinathan-nair-syndrome https://www.malacards.org/card/osteogenesis_imperfecta_retinopathy_seizures_intellectual_disability_syndrome osteogenesis imperfecta retinopathy seizures intellectual deficit Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome is characterized by osteogenesis imperfecta, wormian bones, optic atrophy, retinopathy, seizures and severe developmental delay. It has been described in two sibs born to consanguineous parents. Orphanet:2773 SCTID:722110003 MONDO:0017196 GARD:0000587 MEDGEN:928493 MESH:C535617 Al Gazali Sabrinathan Nair syndrome Al Gazali-Nair syndrome UMLS:C4302824 osteogenesis imperfecta obsolete primary bone dysplasia with decreased bone density hereditary optic atrophy