Osteoporosis-pseudoglioma syndrome

Osteoporosis pseudoglioma syndrome is a very rare autosomal recessive disorder characterized by congenital or infancy-onset blindness and severe juvenile-onset osteoporosis and spontaneous fractures.

Also known as: OPPG, osteoporosis-pseudoglioma syndrome, Ops, osteogenesis imperfecta ocular form, osteogenesis imperfecta, ocular form, osteoporosis pseudoglioma syndrome, pseudoglioma with bone fragility

18 clinical trials for this condition and its sub-types.