Familial dysalbuminemic hyperthyroxinemia combined with Graves’ disease: a rare case report

BACKGROUND: Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant disease characterised by an abnormally increased affinity of albumin for serum thyroxine. Assay interference and differential diagnosis remain challenging for FDH. The condition is more complicated when FDH is combi...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Yuanmeng, Chi, Yue, Chai, Xiaofeng, Liu, He, Li, Naishi, Lian, Xiaolan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583390/
https://www.ncbi.nlm.nih.gov/pubmed/37853391
http://dx.doi.org/10.1186/s12902-023-01481-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583390/
https://www.ncbi.nlm.nih.gov/pubmed/37853391
http://dx.doi.org/10.1186/s12902-023-01481-5

Ejemplares similares