ORPHA:1515
Cranioectodermal dysplasia
Also called CED, Sensenbrenner 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:1515 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Abnormality of the dentition
- Dolichocephaly
- Prominent occiput
- Epicanthus
- Microdontia
- Narrow chest