Cargando…

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

Ejemplares similares

First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant
por: Cho, Yoon Young, et al.
Publicado: (2017)

Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed Entity
por: Dieu, Xavier, et al.
Publicado: (2020)

MON-483 Familial Dysalbuminemic Hyperthyroxinemia with False Hypercortisolemia
por: Chiba, Koki, et al.
Publicado: (2020)

Familial Dysalbuminemic Hyperthyroxinemia as a Cause for Discordant Thyroid Function Tests
por: Ting, Matthew J M, et al.
Publicado: (2021)

Familial Dysalbuminemic Hyperthyroxinemia that was Inappropriately Treated with Thiamazole Due to Pseudo-thyrotoxic Symptoms
por: Fukaishi, Takahiro, et al.
Publicado: (2017)

Clinical, Genetic, and Protein Structural Aspects of Familial Dysalbuminemic Hyperthyroxinemia and Hypertriiodothyroninemia
por: Kragh-Hansen, Ulrich, et al.
Publicado: (2017)

Familial dysalbuminemic hyperthyroxinemia confounding management of coexistent autoimmune thyroid disease
por: Khoo, Serena, et al.
Publicado: (2020)

A Novel Albumin Gene Mutation (R222I) in Familial Dysalbuminemic Hyperthyroxinemia
por: Schoenmakers, Nadia, et al.
Publicado: (2014)

MON-612 Familial Dysalbuminemic Hyperthyroxinemia Cases in Five Unrelated Japanese Families and the Influences on Free T4 Measurement
por: Nagano, Hidekazu, et al.
Publicado: (2019)

Clinical characteristics of familial dysalbuminemic hyperthyroxinemia in Chinese patients and comparison of free thyroxine in three immunoassay methods
por: Zhao, Linlin, et al.
Publicado: (2023)

Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P)
por: Osaki, Yoshinori, et al.
Publicado: (2016)

A Chinese Family with Familial Dysalbuminemic Hyperthyroxinemia (FDH) due to R242H Mutation on Human Albumin Gene: Reevaluating the Role of FDH in Patients with Asymptomatic Hyperthyroxinemia
por: Liu, Hongbing, et al.
Publicado: (2019)

Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia
por: Moran, Carla, et al.
Publicado: (2020)

Analysis of thyroid involvement in children and adult Langerhans cell histiocytosis: An underestimated endocrine manifestation
por: Li, Yuanmeng, et al.
Publicado: (2022)

An Adolescent with Transient Hyperthyroxinemia after Blunt Trauma to Head and Neck
por: Romijn, Michelle, et al.
Publicado: (2021)

MON-481 Remarkable Euthyroid Hyperthyroxinemia Mistaken for Thyrotoxicosis
por: Baghel, Annavi, et al.
Publicado: (2020)

Maternal cognitive function during pregnancy in relation to hypo‐ and hyperthyroxinemia
por: Pop, Victor J., et al.
Publicado: (2019)

MON-480 Isolated Hyperthyroxinemia - Does Everyone Needs Treatment?
por: Bashir, Bilal, et al.
Publicado: (2020)

Anesthetic experience in a clinically euthyroid patient with hyperthyroxinemia and suspected impairment of T4 to T3 conversion: a case report
por: Lee, Sang Hyun, et al.
Publicado: (2014)

Richard Ho-Ping Sia: pioneer of infectiology in China
por: Liu, Xudong, et al.
Publicado: (2022)

Hyperthyroxinemia with a non-suppressed TSH: how to confidently reach a diagnosis in this clinical conundrum
por: Timmons, J. G., et al.
Publicado: (2020)

Wide Spectrum of Thyroid Function Tests in COVID-19: From Nonthyroidal Illness to Isolated Hyperthyroxinemia
por: Hashemipour, Sima, et al.
Publicado: (2022)

Rare presentation of Graves’ disease with myalgia: A case report
por: Kurihara, Masaru, et al.
Publicado: (2021)

Management of Psychosis Associated with Graves' Disease: A Rare Case Report
por: Williams, Ozge Ceren Amuk, et al.
Publicado: (2022)

Rectal Melanoma: Rare Cancer with Grave Prognosis
por: Soufi, Khadija, et al.
Publicado: (2023)

The coexistence of hypercalcemia, osteoporosis and thymic enlargement in graves’ disease: a case report
por: Yan, Dandan, et al.
Publicado: (2020)

Endometriosis in an ectopic kidney: a rare case report and literature review
por: Chen, MengLin, et al.
Publicado: (2023)

Graves' disease: A rare fate of Hashimoto's thyroiditis
por: Jadhav, Rahul, et al.
Publicado: (2020)

Graves’ disease coexisting with resistance to thyroid hormone: a rare case
por: Sun, Hongping, et al.
Publicado: (2017)

Mediastinal Thyroid Carcinoma and Graves' Disease: A Rare Presentation
por: Lomelino Pinheiro, Sara, et al.
Publicado: (2021)

Double trouble – thyro-pericarditis: rare presentation of Graves’ disease as pericarditis—a case report
por: Gondal, Mohsin, et al.
Publicado: (2020)

Very rare case of Graves’ disease with resistance to methimazole: a case report and literature review
por: Mori, Yusaku, et al.
Publicado: (2021)

Graves’ disease with anti-GQ1b antibody syndrome: a rare case report
por: Liang, Tao, et al.
Publicado: (2021)

Coexistence of Primary Hyperaldosteronism and Graves' Disease, a Rare Combination of Endocrine Disorders: Is It beyond a Coincidence—A Case Report and Review of the Literature
por: Gunatilake, S. S. C., et al.
Publicado: (2017)

Tozinameran: Graves' disease: case report
Publicado: (2021)

Tozinameran: Graves' disease: case report
Publicado: (2022)

Tozinameran: Graves' disease : case report
Publicado: (2022)

A rare coexistence of Behcet’s disease and Graves’ thyrotoxicosis in a young man: a case report
por: Joshi, Hareesh, et al.
Publicado: (2020)

Grave's disease associated with immunoglobulin A nephropathy: A rare association
por: Khan, I., et al.
Publicado: (2015)

Graves’ Disease with Pancytopenia and Hepatic Dysfunction: A Rare Case Presentation
por: Behera, Kishore Kumar, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_9ifkjq21jt84v3kp1mqh2skmpd