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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

    craniofacial patient

    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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