ORPHA:93260
Pfeiffer syndrome type 3
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant, Not applicable
- Typical age of onset
- Antenatal, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:93260 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Respiratory distress
- Chiari malformation
- Aqueductal stenosis
- Tracheomalacia
- Short nose
- Depressed nasal bridge