WordNet
- relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
- occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/11/26 14:13:05」(JST)
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- 1. 甲状腺機能正常型高サイロキシン血症および低サイロキシン血症 euthyroid hyperthyroxinemia and hypothyroxinemia
- 2. 甲状腺ホルモンに対する感受性の傷害 impaired sensitivity to thyroid hormone
- 3. 甲状腺刺激ホルモン（TSH）分泌下垂体腺腫 thyrotropin tsh secreting pituitary adenomas
English Journal
- Free thyroxine concentrations in sera of individuals with Familial Dysalbuminemic Hyperthyroxinemia: a comparison of three methods of measurement.
- Refetoff S, Scherberg N, Yuan C, Wu W, Wu Z, McPhaul MJ.
- Thyroid : official journal of the American Thyroid Association. 2019 Dec;().
- Euthyroid individuals with Familial Dysalbuminemic Hyperthyroxinemia (FDH) have often falsely elevated serum free T4 (FT4) concentrations determined by different automated immunoassays. We measured serum FT4 using direct dialysis coupled with tandem mass spectrometry (FT4 DDMS) in individuals with t
- PMID 31822224
- 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.
- Liu H, Ran J, Chen C, Chen G, Zhu P, Tan R, Liu Y.
- International journal of endocrinology. 2019 ;2019()5947415.
- Familial dysalbuminemic hyperthyroxinemia (FDH) has now become an established cause for spurious asymptomatic hyperthyroxinemia. Several different codon mutations on albumin gene had been identified. We here provided an established but rarely reported heterozygous mutation based on gene sequencing r
- PMID 31582975
- Clinical recognition and evaluation of patients with inherited serum thyroid hormone-binding protein mutations.
- Mimoto MS, Refetoff S.
- Journal of endocrinological investigation. 2019 Jul;().
- There are three important thyroid hormone-binding proteins in human serum, thyroxine-binding globulin, transthyretin, and albumin. Genetic variation in these proteins can lead to altered thyroid hormone binding and abnormalities in serum tests of thyroid hormone. Importantly, patients harboring thes
- PMID 31352644
Japanese Journal
- Structural basis of albumin-thyroxine interactions and familial dysalbuminemic hyperthyroxinemia
- PETITPAS I.
- Proc. Natl. Acad. Sci. USA 100, 6440-6445, 2003
- NAID 80016013999
- 家族性異常アルブミン性高サイロキシン血症 : 日本人家系と最近の研究成果
- 千葉 仁志,和田 典男
- 生物物理化学 = Journal of Electrophoresis 44(4), 301-302, 2000-12-15
- NAID 10013221419
Related Links
- Familial dysalbuminemic hyperthyroxinemia information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. ... Familial dysalbuminemic hyperthyroxinemia ...
- To the Editor: Familial dysalbuminemic hyperthyroxinemia (FDH)1 is a well-characterized condition associated with increased circulating total thyroxine (T 4) concentrations and normal physiological thyroid function. It is caused by ...
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★リンクテーブル★
| リンク元 | 「家族性アルブミン異常過チロキシン血症」「家族性アルブミン異常高チロキシン血症」 |
| 関連記事 | 「familial」「hyperthyroxinemia」 |
「家族性アルブミン異常過チロキシン血症」
「家族性アルブミン異常高チロキシン血症」
「familial」
- adj.
- 家族性の、家系性の、家族の