Condition
Pediatric Crouzon Syndrome
What You Need to Know
Crouzon syndrome is a rare birth defect that causes premature closing of several joints in a baby’s skull.
Key Symptoms
Children with Crouzon syndrome may have one or more symptoms, including:
- Misshapen head
- Bulging, wide-set eyes
- Bone deformities in the middle of the face
- Other characteristics
Diagnosis
At Children’s National Hospital, our pediatric team uses the following to diagnosis Crouzon syndrome:
- X-rays
- Diagnostic imaging
- Genetic tests
Treatment
Treatment for Crouzon syndrome focuses on:
- Reducing pressure inside the skull
- Correcting the skull and facial deformities
- Ensuring proper breathing
Schedule an Appointment
Our pediatric specialists provide personalized care for your child’s physical, mental and emotional health needs. Meet our providers and schedule an appointment today.
Frequently Asked Questions
What is Crouzon syndrome?
What causes Crouzon syndrome in children?
What are the symptoms of Crouzon syndrome in children?
How is Crouzon syndrome diagnosed in children?
How is Crouzon syndrome treated in children?
Meet the Providers Who Treat Crouzon Syndrome
Departments that Treat Crouzon Syndrome

Cleft and Craniofacial Program
The Cleft and Craniofacial Program at Children's National unites experts from 10 pediatric fields to offer comprehensive care for children with craniofacial differences, assisting over 400 kids annually. Our team provides convenient, coordinated treatment, ensuring that children receive well-rounded care for their optimal growth and development in one location.

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