Congenital HydrocephalusExams and TestsCongenital hydrocephalus is sometimes diagnosed before birth with a
fetal ultrasound. However, most cases are diagnosed
during a physical exam at or soon after birth. Congenital hydrocephalus usually
is first suspected because of a larger-than-normal head size. A doctor will
also look for other physical signs, such as eyes that almost always look down
and a lot of white showing above the
irises ("sunsetting of the eyes"). A doctor will also
ask about how your baby is eating and sleeping or whether he or she has seemed
fussy. A health professional may request one or more tests to
confirm a diagnosis of congenital hydrocephalus or to further evaluate the
condition. Imaging tests may be used to determine whether extra fluid is
building in the brain, to look at the brain's structure, or to evaluate the
flow of cerebrospinal fluid within and through the brain's ventricles and into
the spinal column. These tests include: Other tests that may be done include:2 - Lumbar puncture, a procedure in which doctors take a sample of cerebrospinal
fluid (CSF). Doctors analyze the CSF sample to see whether an infection may be
causing symptoms. This test helps doctors to measure the pressure of CSF within
the skull. It may also allow some controlled drainage of CSF. A lumbar puncture
usually is only done for
communicating hydrocephalus, which is hydrocephalus
not caused by an obstruction.
- Genetic test,
which examines a
DNA sample to test for abnormal
genes or to analyze the number, arrangement, and
characteristics of the
chromosomes. This may be done if the parents' medical
histories indicate the possibility that a baby has inherited hydrocephalus.
Genetic counseling is recommended along with this
testing.
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