Cargando…

Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P)

Familial dysalbuminemic hyperthyroxinemia (FDH) is a familial autosomal dominant disease caused by mutation in the albumin gene that produces a condition of euthyroid hyperthyroxinemia. In patients with FDH, serum-free thyroxine (FT4) and free triiodothyronine (FT3) concentrations as measured by sev...

Descripción completa

Detalles Bibliográficos
Autores principales:	Osaki, Yoshinori, Hayashi, Yoshitaka, Nakagawa, Yoshinori, Yoshida, Katsumi, Ozaki, Hiroshi, Fukazawa, Hiroshi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Libertas Academica 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821441/ https://www.ncbi.nlm.nih.gov/pubmed/27081329 http://dx.doi.org/10.4137/JCM.S38990

Ejemplares similares

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)

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

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

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)

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)

Familial dysalbuminemic hyperthyroxinemia combined with Graves’ disease: a rare case report
por: Li, Yuanmeng, et al.
Publicado: (2023)

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)

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)

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

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)

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

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)

Inguinal porokeratosis in a Japanese man
por: Hayashi, Yuka, et al.
Publicado: (2013)

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)

COVID-19-associated pulmonary aspergillosis in a Japanese man: A case report
por: Imoto, Waki, et al.
Publicado: (2021)

S218. INSIGHT AND SUBJECTIVITY
por: Monserrat, Clara, et al.
Publicado: (2018)

Do technically efficient surgeons continue to provide active clinical services in a university hospital?
por: Nakata, Yoshinori, et al.
Publicado: (2021)

Association between Visceral or Subcutaneous Fat Accumulation and B-Type Natriuretic Peptide among Japanese Subjects: A Cross-Sectional Study
por: Hayashi, Yoshinori, et al.
Publicado: (2021)

Relationships of Cigarette Smoking and Alcohol Consumption to Metabolic Syndrome in Japanese Men
por: Nakashita, Yumiko, et al.
Publicado: (2010)

Prevalence of and Factors Associated with Smoking among Japanese Medical Students
por: Tamaki, Tetsuo, et al.
Publicado: (2010)

Glycated Albumin versus Glycated Hemoglobin as a Glycemic Indicator in Diabetic Patients on Peritoneal Dialysis
por: Kobayashi, Hiroki, et al.
Publicado: (2016)

Association of Albumin-Bilirubin Grade and Sequential Treatment with Standard Systemic Therapies for Advanced Hepatocellular Carcinoma: A Retrospective Cohort Study Using a Japanese Administrative Database
por: Hiraoka, Atsushi, et al.
Publicado: (2021)

Association between Smoking Habits and Tryptophan Hydroxylase Gene C218A Polymorphism among the Japanese Population
por: Mizuno, Shoichi, et al.
Publicado: (2005)

Fine structure in the α decay of At218
por: Cubiss, J. G., et al.
Publicado: (2019)

High-spin states of $^{218}$Th
por: O'Donnell, D, et al.
Publicado: (2020)

Health Tract, No. 218: Digestibility of Food
Publicado: (1864)

Health Tract, No. 218: Digestibility of Food
Publicado: (1865)

Association of BAP with urinary albumin excretion in postmenopausal, but not premenopausal, non-CKD Japanese women
por: Ozaki, Etsuko, et al.
Publicado: (2018)

Certolizumab Pegol for the Treatment of Moderate to Severe Plaque Psoriasis: 16-Week Results from a Phase 2/3 Japanese Study
por: Umezawa, Yoshinori, et al.
Publicado: (2021)

Microvascular endothelial function in Japanese early adolescents
por: Odanaka, Yutaka, et al.
Publicado: (2017)

TaqMan-MGB SNP genotyping assay to identify 48 citrus cultivars distributed in the Japanese market
por: Endo, Tomoko, et al.
Publicado: (2020)

Efficacy and Safety of Certolizumab Pegol in Japanese Patients with Generalized Pustular Psoriasis and Erythrodermic Psoriasis: 52-Week Results
por: Okubo, Yukari, et al.
Publicado: (2022)

Stem cells from human exfoliated deciduous teeth attenuate mechanical allodynia in mice through distinct from the siglec-9/MCP-1-mediated tissue-repairing mechanism
por: Hayashi, Yoshinori, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_nqljua1ou36atm34f3likjf8ca