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Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown.
Biomarker and diagnostic research for idiopathic congenital hypothyroidism has been reported in the published literature.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for idiopathic congenital hypothyroidism.
4 publications have been identified in PubMed for idiopathic congenital hypothyroidism. Research spans Case Report / Case Series (50%), Diagnostic / Biomarker (25%), and Clinical Trial Publication (25%).
Di Cosmo C (2026). [PMID: 41066039](https://pubmed.ncbi.nlm.nih.gov/41066039/). *Journal of endocrinological investigation*. [Clinical Trial Publication]
Siddiqui MA (2026). [PMID: 41652884](https://pubmed.ncbi.nlm.nih.gov/41652884/). *The British journal of radiology*. [Diagnostic / Biomarker]
Nygren D (2025). [PMID: 40236613](https://pubmed.ncbi.nlm.nih.gov/40236613/). *JCEM case reports*. [Case Report / Case Series]
Yoo S (2024). [PMID: 38822623](https://pubmed.ncbi.nlm.nih.gov/38822623/). *American journal of medical genetics. Part A*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 4:32 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center