Congenital Hypothyroidism
Recent clinical, regulatory, research and industry developments relating to this disease.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Clinical trials
The current development programme across all trial phases.
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Leading journals1
- Thyroid : official journal of the American Thyroid Association1
Leading researchers8
- Bartés B1
- Beauloye V1
- Cassio A1
- Coutant R1
- de Sanctis L1
- Fugazzola L1
- Heinrichs C1
- Krude H1
Affiliations (unnormalised)6
- Centre de Référence des Maladies Rares de la Thyroïde et des Récepteurs Hormonaux1
- Centre de Référence Maladies Endocriniennes de la Croissance et du Développement1
- Centre régional de dépistage néonatal1
- Cliniques Universitaires Saint-Luc1
- Cochin Institute1
- Department of Clinical Sciences and Community Health1
Reference
Authoritative identity, definition & identifiers.
A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.