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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...
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| Vydáno v: | Ann Pediatr Endocrinol Metab |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Korean Society of Pediatric Endocrinology
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6312916/ https://ncbi.nlm.nih.gov/pubmed/30599487 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2018.23.4.235 |
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