Definition
Apert syndrome is a congenital syndrome characterized by craniosynostosis, facial hypoplasia and syndactyly.
Symptoms
- Craniosynostosis
- Facial hypoplasia
- Syndactyly
- Developmental delay
Reasons
FGFR2 gene mutation.
Diagnosis
Clinical findings, genetic testing.
Treatment
Surgical reconstruction.
Which Polyclinic Should You Apply To?
Genetics Polyclinic
What to Do in an Emergency?
In case of increased cranial pressure, emergency services should be consulted.
This page is for general information purposes only.