Cargando…
Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR 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...
Autores principales: | Cho, Won Kyoung, Ahn, Moon-Bae, Jang, Woori, Chae, Hyojin, Kim, Myungshin, Suh, Byung-Kyu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Pediatric Endocrinology
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312916/ https://www.ncbi.nlm.nih.gov/pubmed/30599487 http://dx.doi.org/10.6065/apem.2018.23.4.235 |
Ejemplares similares
-
Report of a family with three generations of undiagnosed familial nonautoimmune hyperthyroidism
por: Stephenson, Alexandra, et al.
Publicado: (2021) -
A Case of Definitive Therapy in Persistent Congenital Hyperthyroidism Secondary to an Activating Variant of the TSHR Gene
por: Reynolds, Sarah M, et al.
Publicado: (2021) -
Long-Term Disproportional TSH Hyposecretion in a Patient With Nonautoimmune Hyperthyroidism After Radioiodine Therapy
por: Nishihara, Eijun, et al.
Publicado: (2023) -
Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene
por: Aycan, Zehra, et al.
Publicado: (2010) -
MON-264 Familial Neonatal Nonautoimmune Hyperthyroidism Due To A Thyrotropin Receptor Gene Mutation (A619G).
por: Taha, Doris, et al.
Publicado: (2019)