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Article

Squamosal Suture Craniosynostosis Due to Hyperthyroidism Caused by an Activating Thyrotropin Receptor Mutation (T632I).

Thyroid : official journal of the American Thyroid Association - 1 Oct 2015

Chawla Reeti, Alden Tord D, Bizhanova Aigerim, Kadakia Rachel, Brickman Wendy, Kopp Peter A

Abstract excerpt

BACKGROUND: Congenital hyperthyroidism can be a cause of failure to thrive, hyperactivity, developmental delay, and craniosynostosis during infancy. Most commonly, the condition occurs in the setting of maternal autoimmune thyroid disease. Rarely, congenital hyperthyroidism can also occur secondary to activating mutations within the thyrotropin (TSH) receptor. PATIENT FINDINGS: A Hispanic male infant presented at...

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Source

Identifiers

PMID: 26114856
DOI: 10.1089/thy.2014.0503

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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