Congenital hypothyroidism laboratory findings: Difference between revisions
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Revision as of 17:49, 20 September 2012
Congenital hypothyroidism Microchapters |
Differentiating Congenital hypothyroidism from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Congenital hypothyroidism laboratory findings On the Web |
American Roentgen Ray Society Images of Congenital hypothyroidism laboratory findings |
Risk calculators and risk factors for Congenital hypothyroidism laboratory findings |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Overview
Laboratory Findings
In the developed world, nearly all cases of congenital hypothyroidism are detected by the newborn screening program. These are based on measurement of TSH or thyroxine (T4) on the second or third day of life. If the TSH is high, or the T4 low, the infant's doctor and parents are called and a referral to a pediatric endocrinologist is recommended to confirm the diagnosis and initiate treatment.