Craniosynostosis

Craniosynostosis is a medical condition in which the skull bones of an infant close prematurely, before the brain is fully formed. This can lead to abnormal growth patterns of the skull and can affect the shape of the head and face.

Causes

Craniosynostosis is usually caused by a genetic mutation. It can be associated with certain genetic syndromes, such as Crouzon syndrome, Apert syndrome, and Pfeiffer syndrome. However, in many cases, the cause of craniosynostosis is unknown.

Symptoms

The most common symptom of craniosynostosis is an abnormally shaped head. Other symptoms can include developmental delays, difficulty feeding, and increased intracranial pressure. In severe cases, craniosynostosis can lead to vision problems, sleep apnea, and other serious health issues.

Diagnosis

Craniosynostosis is usually diagnosed through a physical examination and imaging tests, such as X-rays or CT scans. Genetic testing may also be performed to determine if the condition is associated with a genetic syndrome.

Treatment

Treatment for craniosynostosis usually involves surgery to separate the fused skull bones. This allows the brain to grow normally. In some cases, a helmet may be used after surgery to help shape the skull. Other treatments may include physical therapy and special education services to help with developmental delays.

See also

• Crouzon syndrome
• Apert syndrome
• Pfeiffer syndrome
• Genetic mutation
• Skull
• Brain
• X-ray
• CT scan

Craniosynostosis Resources
Need Help Finding a Doctor? Need help finding a doctor or specialist anywhere in the world? Explore our world directory. WikiMD's DocFinder can assist you in locating millions of physicians.	Medical Knowledge Access the latest research - Most recent articles Ongoing trials.

Translate to: East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski