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Congenital Hyperthyroidism Caused by a Mutation in the Thyrotropin-Receptor Gene

19 Jan 1995

Abstract excerpt

Congenital hyperthyroidism is rare. Most cases occur in infants born of mothers with a history of Graves' disease.1 The disorder is usually transient in such infants, because it is caused by transplacental passage of maternal thyrotropin-receptor–stimulating autoantibodies that are subsequently cleared.2,3 However, a few neonates with persistent nonautoimmune hyperthyroidism of unknown cause have been...

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PMID: 7800007
DOI: 10.1056/nejm199501193320304

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