ORPHA:1465
Coffin-Siris syndrome
Also called CSS
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Antenatal, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1465 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Prominent eyelashes
- Feeding difficulties
- Wide mouth
- Thick lower lip vermilion
- Coarse facial features
- Thick eyebrow