The Full Wiki

More info on Familial dysalbuminemic hyperthyroxinemia

Familial dysalbuminemic hyperthyroxinemia: Wikis


Note: Many of our articles have direct quotes from sources you can cite, within the Wikipedia article! This article doesn't yet, but we're working on it! See more info or our list of citable articles.


From Wikipedia, the free encyclopedia

Familial dysalbuminemic hyperthyroxinemia
Classification and external resources
OMIM 103600
DiseasesDB 32942
MeSH D050010

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

The term was introduced in 1982.[2]


  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. doi:10.1073/pnas.1137188100. PMID 12743361. PMC 164465.  
  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. PMID 6173750.  


Got something to say? Make a comment.
Your name
Your email address