A Case Report of Turner Syndrome with Graves’ Disease during Recombinant Human GH Therapy and Review of Literature
Identifieur interne : 007A63 ( Main/Curation ); précédent : 007A62; suivant : 007A64A Case Report of Turner Syndrome with Graves’ Disease during Recombinant Human GH Therapy and Review of Literature
Auteurs : Makio Nakagawa ; Yasuji Inamo ; Kensuke HaradaSource :
- Clinical Pediatric Endocrinology [ 0918-5739 ] ; 2006.
Abstract
An increased incidence of Hashimoto thyroiditis has been reported in patients with Turner syndrome, but several cases of Graves’ disease were also described ten to 20 years ago. We report the case of a patient with Turner syndrome who developed Graves’ disease, 3 years after successful treatment with recombinant human growth hormone (GH). A diagnosis of Graves’ disease was made and treatment with thiamazole was started, which resulted in normalization of the thyroid function. It is important to monitor thyroid function as well as growth parameters in patients with Turner syndrome.
Url:
DOI: 10.1297/cpe.15.55
PubMed: 24790321
PubMed Central: 4004847
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PMC:4004847Le document en format XML
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<front><div type="abstract" xml:lang="en"><p> An increased incidence of Hashimoto thyroiditis has been reported in patients with
Turner syndrome, but several cases of Graves’ disease were also described ten to 20 years
ago. We report the case of a patient with Turner syndrome who developed Graves’ disease,
3 years after successful treatment with recombinant human growth hormone (GH). A diagnosis
of Graves’ disease was made and treatment with thiamazole was started, which resulted in
normalization of the thyroid function. It is important to monitor thyroid function as well
as growth parameters in patients with Turner syndrome.</p>
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