ORPHA:620113
Non-syndromic unilambdoid craniosynostosis
Also called Isolated occipital plagiocephaly, Isolated unilamboid craniosynostosis, Non-syndromic posterior synostotic plagiocephaly, Non-syndromic unilateral lambdoid synostosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:620113 is classified under "Bone diseases" in the Orphanet nomenclature.