ORPHA:1516
Non-syndromic bilambdoid and sagittal craniosynostosis
Also called BLSS, Bilateral lambdoid and sagittal synostosis, Isolated sagittal and bilambdoid craniosynostosis, Non-syndromic sagittal and bilateral 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:1516 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Macrocephaly
- Dolichocephaly
- Hypertelorism
- Low-set ears
- Craniosynostosis
- Frontal bossing