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.
Comprehensive, easy-to-understand information about this condition
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Organizations with approved therapies for this disease
No approved therapies yet
Research is ongoing — 5 companies have orphan drug designations for this disease
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.
AI-curated news mentioning osteoporosis-pseudoglioma syndrome
Updated Jan 23, 2026
The CDC has released new guidelines aimed at improving osteoporosis prevention and management. These guidelines emphasize the importance of early screening and treatment to reduce fracture risk among at-risk populations.