Hypothyroidism due to TSH receptor mutations

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A type of primary congenital hypothyroidism a permanent thyroid hormone deficiency that is present from birth due to thyroid resistance to TSH.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version May 2024

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Hypothyroidism due to TSH receptor mutations?

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