Rare Zebra

Rare disease search prototype built on Orphanet data

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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