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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Detalles Bibliográficos
Autores principales: Heo, Seung, Jang, Ja-Hyun, Yu, Jeesuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790875/
https://www.ncbi.nlm.nih.gov/pubmed/31607114
http://dx.doi.org/10.6065/apem.2019.24.3.199

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790875/
https://www.ncbi.nlm.nih.gov/pubmed/31607114
http://dx.doi.org/10.6065/apem.2019.24.3.199

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