Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the gene
Most cases of congenital hyperthyroidism are autoimmune forms caused by maternal thyroid stimulating antibodies. Nonautoimmune forms of congenital hyperthyroidism caused by activating mutations of the thyrotropin receptor (TSHR) gene are rare. A woman gave birth to a boy during an emergency cesarean...
Main Authors: | Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh |
---|---|
Format: | Article |
Language: | English |
Published: |
Korean Society of Pediatric Endocrinology
2018-12-01
|
Series: | Annals of Pediatric Endocrinology & Metabolism |
Subjects: | |
Online Access: | http://e-apem.org/upload/pdf/apem-2018-23-4-235.pdf |
Similar Items
-
An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial non-autoimmune hyperthyroidism
by: Jung Hyun Shin, et al.
Published: (2020-12-01) -
Subclinical hyperthyroidism
by: Mohammad Reza Kalantar Hormozi, et al.
Published: (2013-09-01) -
Preoperative Subclinical Hyperthyroidism in Patients With Papillary Thyroid Carcinoma
by: Dongbin Ahn, et al.
Published: (2014-12-01) -
Long-term follow-up result of antithyroid drug treatment of Graves’ hyperthyroidism in a large cohort
by: Meihua Jin, et al.
Published: (2023-03-01) -
Extrathyroidal Manifestations of Persistent Sporadic Non-Autoimmune Hyperthyroidism in a 6-Year-Old Boy: A Case Report
by: Moon Bae Ahn
Published: (2021-07-01)