Literature DB >> 1868606

Prevalence of familial dysalbuminemic hyperthyroxinemia in serum samples received for thyroid testing.

G Arevalo1.   

Abstract

The prevalence of familial dysalbuminemic hyperthyroxinemia (FDH), a condition sometimes mistaken for hyperthyroidism, has not been clearly established. I present a study of the prevalence of FDH in serum samples received for thyroid-function tests in a reference laboratory. A prospective study of 15,674 serum samples was carried out over 24 months, of which 13,232 cases were from women (84.42%) and 2442 were from men (15.58%). FDH was diagnosed in 26 cases, 22 in women and four in men. Therefore, the prevalence of FDH in the total number of samples from both sexes was 0.17%, 0.17% in women, and 0.16% in men, which is consistent with a dominant autosomal type of familial transmission. These findings demonstrate that cases of FDH occur frequently; therefore, every laboratory must be prepared to recognize them and thus avoid an incorrect diagnosis of the patient's thyroid function.

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Year:  1991        PMID: 1868606

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


  5 in total

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4.  A Chinese Family with Familial Dysalbuminemic Hyperthyroxinemia (FDH) due to R242H Mutation on Human Albumin Gene: Reevaluating the Role of FDH in Patients with Asymptomatic Hyperthyroxinemia.

Authors:  Hongbing Liu; Jianmin Ran; Chuping Chen; Guangshu Chen; Ping Zhu; Rongshao Tan; Yan Liu
Journal:  Int J Endocrinol       Date:  2019-09-09       Impact factor: 3.257

5.  Familial dysalbuminaemic hyperthyroxinaemia interferes with current free thyroid hormone immunoassay methods.

Authors:  Serena Khoo; Greta Lyons; Anne McGowan; Mark Gurnell; Susan Oddy; W Edward Visser; Sjoerd van den Berg; David Halsall; Kevin Taylor; Krishna Chatterjee; Carla Moran
Journal:  Eur J Endocrinol       Date:  2020-06       Impact factor: 6.664

  5 in total

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