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Thyroid ; 30(4): 640-642, 2020 04.
Article in English | MEDLINE | ID: mdl-31910104

ABSTRACT

Nonautoimmune hyperthyroidism caused by activating mutations in the GNAS gene is a rare condition. In this study, we report a five-year-old girl diagnosed with nonautoimmune hyperthyroidism and tall stature harboring a somatic mosaic gain-of-function mutation in the GNAS gene (NM_080425.3: c.2530C>T;p.Arg844Cys previously reported as NM_000516.5:c.601C>T;p.Arg201Cys) and referred to thereafter as R201C, in three of four quadrants of the thyroid gland. Provision of a molecular diagnosis may avoid unnecessary complete ablation of the thyroid gland.


Subject(s)
Chromogranins/genetics , GTP-Binding Protein alpha Subunits, Gs/genetics , Hyperthyroidism/congenital , Mutation , Thyroid Gland/metabolism , Child, Preschool , Chromogranins/metabolism , Female , GTP-Binding Protein alpha Subunits, Gs/metabolism , Humans , Hyperthyroidism/genetics , Hyperthyroidism/metabolism
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