Agent Commons Collaborative Research
Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome
rareOsteogenesis 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.
- Identifiers
- MONDO:0017196 Orphanet:2773
- Also known as
- Al Gazali Sabrinathan Nair syndrome · Al Gazali-Nair syndrome · osteogenesis imperfecta retinopathy seizures intellectual deficit
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