ORPHA:1520
Craniofrontonasal dysplasia
Also called CFND, CFNS, Craniofrontonasal syndrome
- Body system
- Bone diseases
- Inheritance pattern
- X-linked dominant
- Typical age of onset
- Antenatal, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:1520 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Depressed nasal ridge
- Craniosynostosis
- Frontal bossing
- Midline defect of the nose
- Ridged fingernail
- Brachycephaly