Literature DB >> 8288714

Postpartum thyroiditis and familial dysalbuminemic hyperthyroxinemia.

W Langsteger1, G Semlitsch, P Költringer, E Meister, O Eber.   

Abstract

Familial dysalbuminemic hyperthyroxinemia (FDH) is a syndrome associated with euthyroidism and increased binding of T4 to serum albumin. The combined occurrence of FDH and postpartum hyperthyroidism due to Graves' disease has only been reported in one patient. We now describe the first case of FDH and thyrotoxicosis due to postpartum silent thyroiditis. In a 19-yr-old woman, FDH, suspected on the basis of strikingly elevated analog free T4 (fT4) and total T4 values, but normal two-step fT4 and serum TSH values, was confirmed by [125I]T4 agarose-gel electrophoresis. When FDH and thyrotoxicosis, characterized by markedly elevated analog fT4, total T4, and two-step fT4 values and undetectable TSH values, coexist, the differential diagnosis may be confusing.

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Year:  1994        PMID: 8288714     DOI: 10.1210/jcem.78.1.8288714

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  1 in total

1.  Familial dysalbuminemic hyperthyroxinemia confounding management of coexistent autoimmune thyroid disease.

Authors:  Serena Khoo; Greta Lyons; Andrew Solomon; Susan Oddy; David Halsall; Krishna Chatterjee; Carla Moran
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2020-02-26
  1 in total

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