How is craniosynostosis diagnosed?
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How is craniosynostosis diagnosed?
Doctors can identify craniosynostosis during a physical exam. A doctor will feel the baby’s head for hard edges along the sutures and unusual soft spots. The doctor also will look for any problems with the shape of the baby’s face.
What happens if craniosynostosis is not treated?
Left untreated, craniosynostosis can result in further cranial deformity and potentially an overall restriction in head growth, with secondary increased intracranial pressure. It can also lead to psychosocial issues as the child interacts with peers during development.
Can craniosynostosis be diagnosed with an MRI?
CONCLUSION. The MRI protocol proposed in this article has the potential to replace CT for the diagnosis and surveillance of craniosynostosis. MRI has excellent soft-tissue resolution and hence is superior to CT in the detection of associated intracranial anomalies and potential complications.
Is craniosynostosis a disease?
Craniosynostosis (kray-nee-o-sin-os-TOE-sis) is a disorder present at birth in which one or more of the fibrous joints between the bones of your baby’s skull (cranial sutures) close prematurely (fuse), before your baby’s brain is fully formed. Brain growth continues, giving the head a misshapen appearance.
Can MRI detect craniosynostosis?
CONCLUSION. The MRI protocol proposed in this article has the potential to replace CT for the diagnosis and surveillance of craniosynostosis. MRI has excellent soft-tissue reso- lution and hence is superior to CT in the detection of associated intracranial anomalies and potential complications.
Can an xray diagnose craniosynostosis?
It showed that X-rays were of little value in diagnosing abnormal skull shapes, especially craniosynostosis, and primary care clinicians should refer concerns to specialist teams. Providing a range of photographs with their detailed diagnosis is particularly useful and is often sufficient for a diagnosis.
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).
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.
