Literature DB >> 3812513

Familial dysalbuminemic hyperthyroxinemia associated with primary thyroid disease.

R A Young, S S Stoffer, L E Braverman.   

Abstract

This study describes a family with intrinsic thyroid disease in addition to familial dysalbuminemic hyperthyroxinemia, a syndrome associated with euthyroidism and increased binding of thyroxine to serum albumin. The simultaneous occurrence of thyroid disease and elevated serum thyroxine concentrations due to familial dysalbuminemic hyperthyroxinemia may confound the diagnosis of the two concurrent disorders and the subsequent therapy of the thyroid disease.

Entities:  

Mesh：

Substances：

Year:  1987        PMID： 3812513     DOI： 10.1016/0002-9343(87)90059-3

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


  2 in total

1.  A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin.

Authors:  P P Yeo; Y Yabu; J R Etzkorn; R Rajatanavin; L E Braverman; S H Ingbar
Journal:  J Endocrinol Invest       Date:  1987-02       Impact factor: 4.256

2.  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
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.