Diagnostic Tests for Microcephaly
Microcephaly Tests: Book Excerpts
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Microcephaly Diagnosis: Book Excerpts
Diagnostic Tests for Microcephaly: Online Medical Books
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for more information about the diagnostic tests for Microcephaly.
Microcephaly:
Diagnostic Approach
(The Diagnostic Approach to Symptoms and Signs in Pediatrics)
Measurehead circumference, weight, and height at each well-child visitusing growth charts published by the CDC (2001).If these measurementsare proportional, child most likely is small in size and does not haveprimary abnormality in brain growth.Head circumference that is proportionallysmaller than weight and length usually signifies primary decreasein brain growth or secondary process (e.g., hypoxic-ischemic encephalopathyor infection). History of microcephaly in family memberssuggests genetic disorder, which is important for genetic counseling.History of maternal drug or alcoholingestion, maternal phenylketonuria, or other disorders should beclarified.Presence of dysmorphic features suggestschromosomal or malformation syndrome, and chromosomal karyotypeshould be determined.Skull radiographs help diagnose craniosynostosis.CT and MRI can diagnose structural defects in brain development.Presence of other findings helps diagnosevarious infections.
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Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006
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