Can a baby with craniosynostosis live a normal life?

Key points about craniosynostosis

Craniosynostosis usually occurs by chance. The first and only symptoms are usually changes in the shape of the baby's head and face. Surgery is usually the recommended treatment. Most children who have surgery early live healthy lives.

Do kids with craniosynostosis live normal lives?

Is it common? Craniosynostosis occurs in one in 2000 births and is often without a known cause. It can sometimes be linked to a genetic syndrome. Most children with craniosynostosis are otherwise healthy and have normal intelligence.

How serious is craniosynostosis in babies?

Each baby born with craniosynostosis is different, and the condition can range from mild to severe. Most babies with craniosynostosis are otherwise healthy.

What are the long term effects of craniosynostosis?

If left untreated, craniosynostosis can lead to serious complications, including: Head deformity, possibly severe and permanent. Increased pressure on the brain. Seizures.

Does craniosynostosis affect brain development?

Craniosynostosis is a condition in which the sutures in a child's skull close too early, causing problems with head growth. Premature closure of the sutures may also cause the pressure inside of the head to increase, which can affect brain development.

Live Q

Do babies with craniosynostosis cry a lot?

Sleepiness or baby is less alert than usual. Very noticeable scalp veins. Increased irritability or fussiness. High-pitched cry.

Does craniosynostosis cause mental retardation?

Chi-square analysis showed no significant differences between rates of retardation or learning disorders based on surgical status. Conclusions: Most children with nonsyndromic craniosynostosis obtain developmental quotients within the normal range in infancy.

What is the life expectancy of someone with craniosynostosis?

People with Crouzon syndrome have a normal life expectancy. Most children with this condition are unaffected intellectually. However, it can alter the shape of the face and cause vision and hearing problems.

Can kids with craniosynostosis play sports?

OBJECTIVE Craniosynostosis (CS) affects about 1 in 2500 infants and is predominantly treated by surgical intervention in infancy. Later in childhood, many of these children wish to participate in sports. However, the safety of participation is largely anecdotal and based on surgeon experience.

Can you get disability for craniosynostosis?

There is no disability listing for Apert syndrome among the Social Security Administration's (SSA's) impairment list.

Is craniosynostosis curable?

Treating craniosynostosis usually involves surgery to unlock and bones and reshape the skull. Historically, craniosynostosis has been treated using surgical methods that involve an incision from ear to ear and the removal, reshaping, and reattachment of affected bones. Sometimes this is still the best option.

How long is recovery after craniosynostosis surgery?

The bones will be healed 6 weeks after surgery but trauma to the head should be avoided. Parents sometimes notice small areas of swelling 8-12 months after surgery as the plates begin to dissolve. Patients undergoing surgery for craniosynostosis are typically seen annually by their surgeons until they are done growing.

Why do babies get craniosynostosis?

Syndromic craniosynostosis is caused by certain genetic syndromes, such as Apert syndrome, Pfeiffer syndrome or Crouzon syndrome, which can affect a baby's skull development. These syndromes usually also include other physical features and health problems.

Can craniosynostosis cause behavior problems?

In unilateral coronal craniosynostosis, problems with intelligence, speech, learning, or behavior have been reported in 52% and 61% of children affected on the left and right sides, respectively⁶⁾.

When does baby head shape become permanent?

It can take 9-18 months before a baby's skull is fully formed. During this time some babies develop positional plagiocephaly. This means that there is a flat area on the back or side of the head. Positional plagiocephaly does not affect brain growth or development; it is purely a shape issue.

How successful is craniosynostosis surgery?

The data support this: in 2020 alone, more than 50 craniosynostosis procedures have been performed, with a success rate of 99%, relatively fast recovery times, and hardly any complications.

How do you fix craniosynostosis?

Is craniosynostosis genetic?

In extremely rare cases, primary isolated craniosynostosis is genetic and in such cases is usually inherited as an autosomal dominant trait. Most cases of primary craniosynostosis that occur as part of a syndrome are also inherited as autosomal dominant traits.

What age is craniosynostosis surgery?

For optimal results, minimally invasive surgery for craniosynostosis should be performed before age 3 months. "However, there are circumstances — such as if the abnormality is milder — that allow us to do minimally invasive surgery successfully even for slightly older children," Dr. Ahn says.

Does mild craniosynostosis need surgery?

A small number of babies with mild craniosynostosis won't need surgical treatment. Rather, they can wear a special helmet to fix the shape of their skull as their brain grows. Most babies with this condition will need surgery to correct the shape of their head and relieve pressure on their brain.

What syndromes are associated with craniosynostosis?

Syndromes most frequently associated with craniosynostosis include Apert, Crouzon, Pfeiffer, Carpenter, and Saethre-Chotzen [1]. Syndromic craniosynostoses are often sporadic and are the result of de novo autosomal dominant mutations involving fibroblast growth factor receptors (FGFRs) and TWIST genes.

Can craniosynostosis come back after surgery?

Re-synostosis after standard surgical procedures for nonsyndromic craniosynostosis is a rare event, which can occur at the same suture or rarely in adjacent sutures.

What is a mild case of craniosynostosis?

Craniosynostosis is a condition in which the sutures (growth seams) in an infant's skull close too early, causing problems with normal brain and skull growth. Non-syndromic craniosynostosis is a non-inherited, isolated finding without related anomalies such as disorders of the limbs, ears or cardiovascular system.

Does craniosynostosis hurt?

In general, craniosynostosis is not a painful condition. However, if there is increased pressure on the brain, it can cause: Abnormalities affecting the face and hands. Headaches.

How common is craniosynostosis?

Craniosynostosis is common and occurs in one out of 2,200 live births. The condition affects males slightly more often than females. Craniosynostosis is most often sporadic (occurs by chance) but can be inherited in some families.