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Congenital Central Hypothyroidism due to a Homozygous Mutation in the TSHβ Subunit Gene
Congenital central hypothyroidism (CCH) is a rare condition occurring in 1 : 20000 to 1 : 50000 newborns. As TSH plasma levels are low, CCH is usually not detected by TSH-based neonatal screening for hypothyroidism, and, as a result, diagnosis is often delayed putting affected children at risk for d...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi Publishing Corporation
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3350182/ https://ncbi.nlm.nih.gov/pubmed/22606512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/369871 |
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