Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in gene

• Main Authors: Seung Heo (Author), Ja-Hyun Jang (Author), Jeesuk Yu (Author)
• Format: Knjiga
• Izdano: Korean Society of Pediatric Endocrinology, 2019-09-01T00:00:00Z.
• Teme: article
• Online dostop: Connect to this object online.

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...