- First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant
-
Cho YY, Song JS, Park HD, Kim YN, Kim HI, Kim TH, Chung JH, Ki CS, Kim SW
- KMID: 2373616
- Ann Lab Med.
- 2017 Jan;37(1):63-65.
- doi: 10.3343/alm.2017.37.1.63
Familial dysalbuminemic hyperthyroxinemia (FDH) is an inherited disease characterized by increased circulating total thyroxine (T4) levels and normal physiological thyroid function. Heterozygous albumin gene (ALB) variants have been reported to... -
- CITED
-
- Close
- SHARE
-
- Close
