Craniosynostosis
Overview: Craniosynostosis is a congenital condition in which the bones in an infant’s skull fuse too early, preventing normal growth of the brain and affecting the shape of the head.
Symptoms
Common symptoms of craniosynostosis include an abnormal head shape, delayed development of motor skills, developmental delays, and abnormal skull growth patterns. In severe cases, increased pressure in the skull can also lead to vision problems and increased intracranial pressure.
Causes
Craniosynostosis is caused by a genetic mutation that affects the normal growth and development of the skull. Other factors that may increase the risk of developing craniosynostosis include prenatal exposure to certain medications, maternal infections during pregnancy, and exposure to environmental toxins.
FAQ’s
Is craniosynostosis a rare condition?
Craniosynostosis is not a rare condition, and it affects about 1 in every 2,000 to 2,500 live births.
Is craniosynostosis a hereditary condition?
Yes, craniosynostosis can be treated through surgery to correct the abnormal head shape and relieve pressure on the brain.
Can craniosynostosis be treated?
Craniosynostosis can be hereditary in some cases, but it can also occur in infants without a family history of the condition.
Can craniosynostosis affect a child's intellectual development?
In some cases, craniosynostosis can affect a child’s intellectual development if the pressure on the brain interferes with normal brain function. However, with prompt treatment, most children with craniosynostosis have a good prognosis for normal development.
Is craniosynostosis a life-threatening condition?
Craniosynostosis itself is not a life-threatening condition, but if left untreated, the increased pressure in the skull can lead to serious complications such as brain damage, vision problems, and developmental delays.
