A Novel Mutation in the Albumin Gene (R218S) Causing Familial Dysalbuminemic Hyperthyroxinemia in a Family of Bangladeshi Extraction

Background: Familial dysalbuminemic hyperthyroxinemia (FDH) is a common cause of euthyroid hyperthyroxinemia. Clinical recognition of FDH is crucial for preventing unnecessary therapy in clinically euthyroid patients with abnormal thyroid function tests. Our goal was to identify the cause of abnorma...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Greenberg, Solomon Maximo, Ferrara, Alfonso Massimiliano, Nicholas, Everton S., Dumitrescu, Alexandra M., Cody, Vivian, Weiss, Roy E., Refetoff, Samuel
Format: Artigo
Sprog:Inglês
Udgivet: Mary Ann Liebert, Inc. 2014
Fag:
Original StudiesThyroid Dysfunction: Hypothyroidism, Thyrotoxicosis, and Thyroid Function Tests
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4046191/
https://ncbi.nlm.nih.gov/pubmed/24494774
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/thy.2013.0540
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker