NIH GARD Information: Oslam syndrome
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
- Osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anemia
- Osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.