ORPHA:2760
OSLAM syndrome
Also called Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2760 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Carious teeth
- Abnormality of neutrophils
- Osteosarcoma
- Increased mean corpuscular volume
- Short stature
- Radioulnar synostosis