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A condition associated with reduced active import of iodide across the basolateral membrane of the follicular cells of the thyroid gland. Inactivating mutations in the SLC5A5 gene encoding the sodium-iodide symporter are responsible for the condition.
No clinical trials have been registered for hypothyroidism due to iodide transport defect.
3 publications have been identified in PubMed for hypothyroidism due to iodide transport defect. Research spans Case Report / Case Series (67%) and Review / Meta-Analysis (33%).
Abe K (2025). [PMID: 39895319](https://pubmed.ncbi.nlm.nih.gov/39895319/). *Thyroid*. [Case Report / Case Series]
Korkmaz HA (2025). [PMID: 39857886](https://pubmed.ncbi.nlm.nih.gov/39857886/). *Children (Basel)*. [Review / Meta-Analysis]
Carro GH (2024). [PMID: 39749016](https://pubmed.ncbi.nlm.nih.gov/39749016/). *Front Endocrinol (Lausanne)*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 11:13 AM UTC
Genetic and Rare Diseases Info Center