Clinical characteristics of familial dysalbuminemic hyperthyroxinemia in Chinese patients and comparison of free thyroxine in three immunoassay methods [PDF]
Frontiers in Endocrinology, 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 ...
Yanyan Zhao, Shoujun Wang
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An Adolescent with Transient Hyperthyroxinemia after Blunt Trauma to Head and Neck
Case Reports in Endocrinology, 2021 Background. Thyroid storm is a well-known complication of surgical procedures in the lower neck, but is rare after a blunt neck trauma. The cases described previously have mainly focussed on adults with pre-existent thyroid disease.
Michelle Romijn +3 more
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Familial dysalbuminemic hyperthyroxinemia combined with Graves’ disease: a rare case report [PDF]
BMC Endocrine Disorders, 2023 Background Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant disease characterised by an abnormally increased affinity of albumin for serum thyroxine. Assay interference and differential diagnosis remain challenging for FDH.
Yuanmeng Li +5 more
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Coexistence of familial dysalbuminemic hyperthyroixinemia and papillary thyroid carcinoma: a rare case report and diagnostic challenge [PDF]
Therapeutic Advances in Endocrinology and MetabolismFamilial dysalbuminemic hyperthyroxinemia (FDH) is a form of euthyroid hyperthyroxinemia caused by ALB gene variants that is commonly misdiagnosed in clinical practice. When coexisting with papillary thyroid carcinoma (PTC), this condition may complicate
Yajie Li +4 more
doaj +2 more sources
Frontiers in Endocrinology, 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.
Mónica Galliano +2 more
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Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia [PDF]
Thyroid, 2020 A 23-year-old man and his grandmother with hyperthyroxinemia and hypercortisolemia were heterozygous for an ALB mutation (p. Arg218Pro), known to cause familial dysalbuminemic hyperthyroxinemia (FDH).
Mark Gurnell +2 more
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Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed Entity [PDF]
Journal of Clinical Medicine, 2020 Resistance to thyroid hormone (RTH) is a syndrome characterized by impaired sensitivity of tissues to thyroid hormone (TH). The alteration of TH-binding proteins, such as in Familial Dysalbuminemic Hyperthyroxinemia (FDH), can mimic the abnormal serum thyroid tests typical of RTH.
Patrice Rodien +2 more
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Incidental detection of hereditary bisalbuminemia in a patient with positive DAT coombs: A case-based review [PDF]
Metabolism OpenBisalbuminemia is a rare, typically benign condition marked by the presence of a bifid albumin band on serum protein electrophoresis. It can either be inherited due to a point mutation or acquired in association with various medical conditions, most ...
Elena Avgoustou +5 more
doaj +2 more sources
Medičnì Perspektivi, 2023 The search for a connection between changes in the indicators of the pro-oxidant system of brain structures and the thyroid gland as a target organ is an urgent issue.
Ya.S. Voichenko, O.H. Rodynskyi
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Anesthetic experience in a clinically euthyroid patient with hyperthyroxinemia and suspected impairment of T4 to T3 conversion: a case report [PDF]
Korean Journal of Anesthesiology, 2014 We report an anesthetic experience in a clinically euthyroid patient with hyperthyroxinemia (elevated free thyroxine, fT4 and normal 3, 5, 3'-L-triiodothyronine, T3) and suspected impairment of conversion from T4 to T3.
Sang Hyun Lee +6 more
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