ORPHA:1906
Fetal valproate spectrum disorder
Also called Fetal valproate syndrome, Fetal valproic acid syndrome, Valproic acid embryopathy
- Body system
- Bone diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Antenatal, Childhood, Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:1906 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Narrow mouth
- Thin vermilion border
- Epicanthus
- Long philtrum
- Depressed nasal ridge
- Omphalocele