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...

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Detalhes bibliográficos
Main Authors: Greenberg, Solomon Maximo, Ferrara, Alfonso Massimiliano, Nicholas, Everton S., Dumitrescu, Alexandra M., Cody, Vivian, Weiss, Roy E., Refetoff, Samuel
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2014
Assuntos:
Original StudiesThyroid Dysfunction: Hypothyroidism, Thyrotoxicosis, and Thyroid Function Tests
Acesso em linha: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
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