Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia.
Albumins
/ chemistry
Genotype
Heterozygote
Humans
Hydrocortisone
/ blood
Hyperthyroxinemia
/ complications
Hyperthyroxinemia, Familial Dysalbuminemic
/ complications
Immunoassay
Male
Military Personnel
Mutation
Protein Binding
Serum Albumin
/ genetics
Serum Albumin, Human
/ genetics
Steroids
/ chemistry
Thyronines
/ blood
Thyroxine
/ blood
Young Adult
albumin
assay interference
discordant thyroid function tests
familial dysalbuminemic hyperthyroxinemia
hypercortisolemia
Journal
Thyroid : official journal of the American Thyroid Association
ISSN: 1557-9077
Titre abrégé: Thyroid
Pays: United States
ID NLM: 9104317
Informations de publication
Date de publication:
11 2020
11 2020
Historique:
pubmed:
17
7
2020
medline:
9
11
2021
entrez:
17
7
2020
Statut:
ppublish
Résumé
A 23-year-old man and his grandmother with hyperthyroxinemia and hypercortisolemia were heterozygous for an
Identifiants
pubmed: 32669045
doi: 10.1089/thy.2020.0315
pmc: PMC7692891
doi:
Substances chimiques
ALB protein, human
0
Albumins
0
Serum Albumin
0
Steroids
0
Thyronines
0
Thyroxine
Q51BO43MG4
Hydrocortisone
WI4X0X7BPJ
Serum Albumin, Human
ZIF514RVZR
Types de publication
Case Reports
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1681-1684Subventions
Organisme : Medical Research Council
ID : G0600717
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00014/5
Pays : United Kingdom
Références
J Clin Endocrinol Metab. 2000 Aug;85(8):2786-92
pubmed: 10946882
Best Pract Res Clin Endocrinol Metab. 2015 Oct;29(5):735-47
pubmed: 26522458
Chem Phys Lipids. 2017 Oct;207(Pt B):271-278
pubmed: 28435101
J Clin Endocrinol Metab. 1997 Oct;82(10):3246-50
pubmed: 9329347