Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome

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.

Also known as: Al Gazali-Nair syndrome, Al Gazali Sabrinathan Nair syndrome, osteogenesis imperfecta retinopathy seizures intellectual deficit

33 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome itself.