ORPHA:1225
Baller-Gerold syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Antenatal, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1225 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Finger aplasia
- Large fontanelles
- Brachyturricephaly
- Brachycephaly
- Proptosis
- Growth delay