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Athyreosis is a form of thyroid dysgenesis characterized by complete absence of thyroid tissue that results in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth.
Biomarker and diagnostic research for athyreosis has been reported in the published literature.
Estimated prevalence: 1-9 in 100,000 (Uncommon).
No clinical trials have been registered for athyreosis.
1 publication has been identified in PubMed for athyreosis. Research spans Diagnostic / Biomarker (100%).
Sumathy S (2024). [PMID: 39881764](https://pubmed.ncbi.nlm.nih.gov/39881764/). *Indian journal of endocrinology and metabolism*. [Diagnostic / Biomarker]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 2:49 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center