Literature DB >> 3767254

Thyroid function tests in patients with familial dysalbuminaemic hyperthyroxinaemia (FDH).

M F Stewart, W A Ratcliffe, I Roberts.   

Abstract

Two patients with familial dysalbuminaemic hyperthyroxinaemia (FDH) are described in whom the albumin variant resulted in raised total T4 levels, and artefactually raised free T4 using a 'single-step' technique employing an analogue of T4 as tracer. The first patient was clinically euthyroid and presented with relapse of schizophrenia and abnormal thyroid function tests (total T4 336 nmol/L, total T3 4.2 nmol/L, TSH 1.8 mU/L, free T4 73 pmol/L). These results led to diagnostic confusion and the patient was treated with a short course of anti-thyroid drugs. The second patient had signs and symptoms of thyrotoxicosis at her first visit but was clinically euthyroid 5 months later when she was 10 weeks pregnant. Thyroid function tests were total T4 259 nmol/L, total T3 3.6 nmol/L, TSH 3.8 mU/L, free T4 46 pmol/L. Further studies showed both patients to be biochemically euthyroid. A variant albumin was confirmed in both patients by a screening test for FDH and by reverse-flow electrophoresis. Family studies on 10 relatives of the first patient identified eight with FDH. A simple screening procedure for the indentification of FDH is described and the use of laboratory tests in suspected cases is discussed.

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Year:  1986        PMID: 3767254     DOI: 10.1177/000456328602300107

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  4 in total

1.  Analytical and clinical evaluation of a new one-step non-analogue radioimmunoassay for serum-free thyroxine.

Authors:  R Sapin; F Gasser; J L Schlienger; J Chambron
Journal:  Eur J Nucl Med       Date:  1990

2.  Familial dysalbuminaemic hyperthyroxinaemia.

Authors:  S J Fleming; G F Applegate; C G Beardwell
Journal:  Postgrad Med J       Date:  1987-04       Impact factor: 2.401

3.  Familial dysalbuminaemic hyperthyroxinaemia and other causes of euthyroid hyperthyroxinaemia.

Authors:  C Farror; M L Wellby; C Beng
Journal:  J R Soc Med       Date:  1987-12       Impact factor: 18.000

4.  A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia.

Authors:  Nadia Schoenmakers; Carla Moran; Irene Campi; Maura Agostini; Olivia Bacon; Odelia Rajanayagam; John Schwabe; Sonia Bradbury; Timothy Barrett; Frank Geoghegan; Maralyn Druce; Paolo Beck-Peccoz; Angela O'Toole; Penelope Clark; Michelle Bignell; Greta Lyons; David Halsall; Mark Gurnell; Krishna Chatterjee
Journal:  J Clin Endocrinol Metab       Date:  2014-03-19       Impact factor: 5.958

  4 in total

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