ORPHA:1553
Curry-Jones syndrome
Also called Corpus callosum agenesis-polysyndactyly syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1553 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Hypertelorism
- Hypopigmented skin patches
- Finger syndactyly
- Facial asymmetry
- Microphthalmia
- Intellectual disability