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Updated: Feb 22, 2026

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An Ex vivo Culture System to Study Thyroid Development
Published on: June 6, 2014
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Thyroid Function Testing in Neonates With Maternal History of Disease
Lisa Underland1, Lisa Kenigsberg2, Kristina M Derrick1
11 Children's Hospital at Montefiore, Bronx, NY, USA.
Clinical Pediatrics
|September 22, 2017
Summary
Maternal thyroid disease can lead to congenital hypothyroidism. Some infants need further testing beyond newborn screening, as thyroid levels fluctuate significantly after birth.
Area of Science:
- Neonatal Medicine
- Endocrinology
- Pediatrics
Background:
- Maternal thyroid disease poses a risk for congenital hypothyroidism in newborns.
- Thyroid-stimulating hormone (TSH) blocking antibodies are a known cause.
- Current guidelines lack specific testing protocols beyond initial newborn screening.
Purpose of the Study:
- To evaluate the necessity of additional thyroid function testing in infants with a maternal history of thyroid disease.
- To identify infants who may be missed by standard newborn screening protocols.
Main Methods:
- Retrospective chart review of 561 newborns with thyroid function tests due to maternal thyroid disease history.
- Assessment of thyroid disease status in 352 infants.
- Analysis of newborn screening data.
Main Results:
- Seven infants were diagnosed with hypothyroidism.
- Three of these infants had negative newborn screening results.
- These three infants required prolonged levothyroxine treatment, indicating persistent hypothyroidism.
Conclusions:
- Infants born to mothers with thyroid disease may require follow-up thyroid function testing beyond the standard newborn screen.
- Delayed testing after initial thyroid level stabilization may be beneficial.
- Early identification and treatment are crucial for managing congenital hypothyroidism.
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