Familial dysalbuminemic hyperthyroxinemia

Familial dysalbuminemic hyperthyroxinemia is a type of hyperthyroxinemia associated with mutations in the human serum albumin gene.[1]

Familial dysalbuminemic hyperthyroxinemia
SpecialtyEndocrinology

The term was introduced in 1982.[2]

References
  1. Petitpas I, Petersen CE, Ha CE, et al. (May 2003). "Structural basis of albumin–thyroxine interactions and familial dysalbuminemic hyperthyroxinemia". Proc. Natl. Acad. Sci. U.S.A. 100 (11): 6440–5. Bibcode:2003PNAS..100.6440P. doi:10.1073/pnas.1137188100. PMC 164465. PMID 12743361.
  2. Ruiz M, Rajatanavin R, Young RA, et al. (March 1982). "Familial dysalbuminemic hyperthyroxinemia: a syndrome that can be confused with thyrotoxicosis". N. Engl. J. Med. 306 (11): 635–9. doi:10.1056/NEJM198203183061103. PMID 6173750.
Classification


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.