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MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation
Background. Congenital hypothyroidism (CH) is most frequently caused by thyroid dysgenesis. Approximately 2% of cases with thyroid dysgenesis are familial. TSH receptor (TSHR) gene mutations have been reported in patients with thyroid gland dysgenesis; however, they are not known to be associated wi...
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| Publicado en: | J Endocr Soc |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Endocrine Society
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6551143/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-265 |
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