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Congenital hypothyroidism and thyroid dyshormonogenesis: a case report of siblings with a newly identified mutation in thyroperoxidase
BACKGROUND: Thyroid dyshormonogenesis continues to be a significant cause of congenital hypothyroidism. Over time, forms of thyroid dyshormonogenesis can result in goiter, which can lead to difficult management decisions as the pathologic changes can both mimic or lead to thyroid cancer. METHODS: He...
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| Izdano u: | J Pediatr Endocrinol Metab |
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| Glavni autori: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2016
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4853235/ https://ncbi.nlm.nih.gov/pubmed/26894573 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/jpem-2015-0253 |
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