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Incidence:
Diagnosis: The diagnosis begins with an examination by a
pediatrician, pediatric neurosurgeon or craniofacial surgeon. A primary
objective of the examination is to rule out
craniosynostosis
(a condition that requires surgical correction). The initial examination involves questions about
gestation, birth, in utero and post-natal positioning (for example,
sleeping position). The physical examination includes inspection of the
infant's head and may involve palpation (carefully feeling) of the
child's skull for
suture ridges and soft
spots (the
fontanelles).
The physician may also request x-rays or computerized tomography (a CAT
scan, a series of photographic images of the skull). These images provide the most reliable method
for diagnosing premature fusion of the
sagittal suture (craniosynostosis). In
addition, the physician may make (or order) a series of measurements
from the child's face and head [more on
cranial
anthropometry]. These measurements will be used to assess severity
and monitor treatment.
Treatment: The treatment of
scaphocephaly depends upon the etiology (cause) of the
condition:
- Scaphocephaly resulting from fusion of the
sagittal suture (craniosynostosis)
must
be treated
surgically. Parents should consult a pediatric neurosurgeon or a
craniofacial surgeon to discuss treatment option.
- Depending upon severity,
scaphocephaly resulting
from external/positional deformation can be treated with repositioning
and/or head banding. Parents should consult a pediatrician, a
pediatric neurosurgeon or a craniofacial surgeon for information on
repositioning and/or for referral and a prescription for head
banding.
Support Groups:
Parent/Child Experiences
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