Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in 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...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Korean Society of Pediatric Endocrinology
2019-09-01
|
| Sarja: | Annals of Pediatric Endocrinology & Metabolism |
| Aiheet: | |
| Linkit: | http://e-apem.org/upload/pdf/apem-2019-24-3-199.pdf |
| Tagit: |
Ei tageja, Lisää ensimmäinen tagi!
|