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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Familial dysalbuminemic hyperthyroxinemia: a study of four probands and the kindred of three.

We investigated four probands, and the kindred of three, with familial dysalbuminemic hyperthyroxinemia, using the one- and two-step tests for free thyroxin and other thyroid-function tests. The results indicate that this is an autosomal dominant trait. The discovery of eight cases in our patient population, which represents about 4% of our hyperthyroxinemic patients (8/320), during eight months indicates that this aberration is more common than suspected. Its importance lies in the misinterpretation of test results and the consequent inappropriate treatment for thyrotoxicosis.[1]

References

  1. Familial dysalbuminemic hyperthyroxinemia: a study of four probands and the kindred of three. Scottolini, A.G., Bhagavan, N.V., Oshiro, T., Powers, L. Clin. Chem. (1984) [Pubmed]
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