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OSLAM syndrome

MeSH: C537138ORPHA: 2760

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

OSLAM syndrome is characterised by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangy, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anaemia

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with OSLAM syndrome, sourced from HPO and Orphanet clinical annotations.

Carious teethAbnormality of neutrophilsOsteosarcomaRadioulnar synostosisClinodactyly of the 5th fingerShort statureIncreased mean corpuscular volume

Classification & Codes

MeSH Code

C537138

Orphanet Code

ORPHA:2760
OSLAM syndrome
MeSHC537138
OrphanetORPHA:2760
Treatments0 drug(s)
Symptoms on record7 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO