ORPHA:560
Marshall syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant, Autosomal recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:560 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Abnormality of the dentition
- Thick lower lip vermilion
- Thick upper lip vermilion
- Brachycephaly
- Malar flattening
- Hypertelorism