Familial dysalbuminemic hyperthyroxinemia coexisting with a Grave's disease: a Belgian case report

Clin Chem Lab Med. 2024 Apr 2;62(9):e197-e199. doi: 10.1515/cclm-2024-0204. Print 2024 Aug 27.

Authors

Fleur Wolff¹, Françoise Fery², Julie Désir³, Romy Gadisseur⁴, Etienne Cavalier⁴, Frédéric Cotton¹

Affiliations

¹ Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles (LHUB-ULB), Université Libre de Bruxelles (ULB), Brussels, Belgium.
² Department of Endocrinology, Centre Hospitalier Interrégional Edith Cavell (CHIREC), Brussels, Belgium.
³ Human Genetics Center, Institute of Pathology and Genetics, Gosselies, Belgium.
⁴ Department of Clinical Chemistry, CHU de Liège, CIRM, University of Liège (ULiège), Liège, Belgium.

PMID: 38557642
DOI: 10.1515/cclm-2024-0204

No abstract available

Keywords: Grave’s disease; high affinity HSA variants; hyperthyroxinemia.

Publication types

Case Reports
Letter

MeSH terms

Adult
Belgium
Female
Graves Disease* / blood
Graves Disease* / complications
Graves Disease* / diagnosis
Humans
Hyperthyroxinemia, Familial Dysalbuminemic* / blood
Hyperthyroxinemia, Familial Dysalbuminemic* / diagnosis
Male