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Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene
Congenital hypothyroidism (CH) is the most common endocrine disorder in neonates and infants with an incidence of one in 2,000 to one in 4,000 newborns. Primary CH can be caused by thyroid dysgenesis and thyroid dyshormonogenesis. CH due to a TG gene mutation is one cause of thyroid dyshormonogenesi...
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| Gepubliceerd in: | Ann Pediatr Endocrinol Metab |
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| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Korean Society of Pediatric Endocrinology
2019
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6790875/ https://ncbi.nlm.nih.gov/pubmed/31607114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2019.24.3.199 |
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