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Pendred syndrome with hyperthyroidism
Objectives: Pendred syndrome is an autosomal recessive disorder characterized by the combination of sensorineural deafness and goiter and is caused by biallelic mutations in the SLC26A4/PDS gene. Thyroid function is generally reported as euthyroid or hypothyroid in this condition. We present a case...
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| Publicado no: | J Rural Med |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Japanese Association of Rural Medicine
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7530597/ https://ncbi.nlm.nih.gov/pubmed/33033545 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2185/jrm.2020-011 |
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