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MATERNAL GRAVES DISEASE AND ABNORMAL CYP2D6 GENOTYPE WITH FETAL HYPERTHYROIDISM
OBJECTIVE: Fetal hyperthyroidism is a rare yet potentially fatal complication of past or present maternal Graves disease (GD). Our objective was to present a unique case of fetal hyperthyroidism in a mother with a prior history of GD and a cytochrome P450 2D6 (CYP2D6) polymorphism. METHODS: The clin...
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| Pubblicato in: | AACE Clin Case Rep |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Association of Clinical Endocrinologists
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7357613/ https://ncbi.nlm.nih.gov/pubmed/32671217 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4158/ACCR-2019-0517 |
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