Rare Zebra

Rare disease search prototype built on Orphanet data

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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