Zobrazeno 1 - 10
of 103
pro vyhledávání: '"euthyroid hyperthyroxinemia"'
Autor:
Linlin Zhao, Yingying Zhou, Fengjiao Huang, Xiaoyang He, Guili Mei, Shoujun Wang, Yanyan Zhao
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveFamilial dysalbuminemic hyperthyroxinemia (FDH) has not been thoroughly studied in the Chinese population to date. The clinical characteristics of FDH in Chinese patients were summarized, and the susceptibility of common free thyroxine (FT4)
Externí odkaz:
https://doaj.org/article/224b0b0a77364b48b73bdc667fa59fe1
Publikováno v:
Frontiers in Endocrinology, Vol 8 (2017)
Familial dysalbuminemic hyperthyroxinemia (FDH-T4) and hypertriiodothyroninemia (FDH-T3) are dominantly inherited syndromes characterized by a high concentration of thyroid hormone in the blood stream. The syndromes do not cause disease, because the
Externí odkaz:
https://doaj.org/article/db0fba34091b44d0b7a2b11f7e99143a
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:1201-1205
Objectives Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant condition caused by heterozygous gain-of-function mutations in the human ALB gene. Case presentation We report, a three-year-old boy with FDH due to p.R242P (or p.R21
Publikováno v:
Journal of the Endocrine Society
Introduction Discordant thyroid function tests are routinely encountered in clinical practice. Differential diagnoses include acute thyroxine (T4) ingestion, laboratory interference from heterophilic antibodies, thyroid hormone resistance, thyroid-st
Akademický článek
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Autor:
Annavi Baghel, Joshua D Maier
Publikováno v:
Journal of the Endocrine Society
CLINICAL CASE A 46 year old caucasian female with past medical history of menorrhagia was referred from primary care for evaluation of thyrotoxicosis. Thyroid function was assessed in the context of menometrorrhagia. She did not have any history of t
Autor:
Alexander M. Menzies, Roderick J. Clifton-Bligh, Richard A. Scolyer, Georgina V. Long, Christopher A. Muir, Venessa H M Tsang
Publikováno v:
Journal of the Endocrine Society
Background: Thyroid toxicity is common following immune checkpoint inhibitor (ICI) treatment. Published studies estimate the incidence at 10-20%, although rates vary widely between different ICIs. The etiology of ICI-associated thyroid immune related
Akademický článek
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Autor:
Tomoaki Sato, Isao Kurihara, Taeko Shimizu, Jaeduk Yoshimura Noh, Sakiko Kobayashi, Hiroshi Itoh, Kiminori Sugino, Koichi Ito
Publikováno v:
Endocrine Journal. 64:207-212
Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant condition and is the most commonly inherited euthyroid hyperthyroxinemia in Caucasians. However, it is extremely rare in Asian populations. A 30-year-old Japanese woman, who was
Publikováno v:
Open Journal of Obstetrics and Gynecology. :623-638
Hypothyroidism, defined as thyrotropin (TSH) above and free thyroxine (fT4) serum level below the reference rage, as well as hyperthyroidism, defined as suppressed TSH and elevated thyroid hormones exceeding the upper limit of the reference range, ma