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A rare case of Turner\'s syndrome with thyroid associated orbitopathy

Year: 2024
Type: article
Study design: Case Report
Abstract: Turner syndrome (TS) is a chromosomal disorder that occurs in 1 per 2500 live-born females, due to complete or partial absence of a second normal X chromosome resulting in short stature and ovarian failure. The risk of autoimmune diseases in patients with TS is quite prominent, especially autoimmune thyroiditis.Nevertheless, Graves’ disease (GD) has been rarely reported in Turner’s syndrome with 45, XO karyotype. Here we report a case of adult phenotypic female who first time presented with Graves’ orbitopathy and later was diagnosed to have Turner’s syndrome.
Language: English
Field: Medicine
Open Access status: diamond
OpenAlex ID: W4402989197
FWCI:
Cites: 14
Cited by:
Related to: 10