ORPHA:87
Apert syndrome
Also called ACS1, Acrocephalosyndactyly type 1
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Antenatal, Neonatal
- Estimated prevalence
- Unknown (Europe)
- Rarity class
- Unknown
ORPHA:87 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Brachyturricephaly
- Hypoplasia of the maxilla
- Broad forehead
- Conductive hearing impairment
- Proptosis
- Craniosynostosis