Familial dysalbuminemic hyperthyroxinemia

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]

Familial dysalbuminemic hyperthyroxinemia
Specialty	Endocrinology

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.

External links

Classification	D OMIM: 103600 MeSH: D050010 DiseasesDB: 32942