Adverts

Open Access Articles- Top Results for Familial dysalbuminemic hyperthyroxinemia

Familial dysalbuminemic hyperthyroxinemia

Familial dysalbuminemic hyperthyroxinemia
Classification and external resources
OMIM 103600
DiseasesDB 32942
NCI Familial dysalbuminemic hyperthyroxinemia
Patient UK Familial dysalbuminemic hyperthyroxinemia
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]

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. PMC 164465. PMID 12743361. doi:10.1073/pnas.1137188100. 
  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. doi:10.1056/NEJM198203183061103. 

Lua error in package.lua at line 80: module 'Module:Buffer' not found.