congenital dysfibrinogenemia

先天性異常フィブリノゲン血症

WordNet

1. present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate

PrepTutorEJDIC

1. (病気・身体的欠陥など)生まれつきの,先天的な

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• 1. フィブリノゲンの異常 disorders of fibrinogen
• 2. 静脈血栓症の原因の概要 overview of the causes of venous thrombosis
• 3. 血漿分画製剤および組換えDNA産生凝固因子 plasma derivatives and recombinant dna produced coagulation factors
• 4. 肝疾患患者における止血異常 hemostatic abnormalities in patients with liver disease
• 5. 出血性素因を有する成人患者へのアプローチ approach to the adult patient with a bleeding diathesis

English Journal

• Natural history of patients with congenital dysfibrinogenemia.

• Casini A1, Blondon M1, Lebreton A1, Koegel J2, Tintillier V3, de Maistre E4, Gautier P5, Biron C6, Neerman-Arbez M2, de Moerloose P7.
• Blood.Blood.2014 Oct 15. pii: blood-2014-06-582866. [Epub ahead of print]
• We conducted a multicentre study of 101 subjects with Congenital Dysfibrinogenemia (CD) to characterize the incidence of hemorrhagic and thrombotic events as well as complications of pregnancy and surgery. At the time of diagnosis, 10.9% and 13.9% had experienced major bleeding and thrombotic events
• PMID 25320241

• Two novel mutations in the fibrinogen γ nodule.

• Kotlín R1, Pastva O2, Stikarová J2, Hlaváčková A2, Suttnar J2, Chrastinová L2, Riedel T3, Salaj P2, Dyr JE2.
• Thrombosis research.Thromb Res.2014 Oct;134(4):901-8. doi: 10.1016/j.thromres.2014.07.021. Epub 2014 Jul 21.
• INTRODUCTION: Congenital dysfibrinogenemia and hypofibrinogenemia are rare diseases characterized by inherited abnormality in the fibrinogen molecule, resulting in functional defects (dysfibrinogenemia) or low fibrinogen plasma levels (hypofibrinogenemia).MATERIALS AND METHODS: We have described two
• PMID 25074738

• Thromboelastographic phenotypes of fibrinogen and its variants: clinical and non-clinical implications.

• Galanakis DK1, Neerman-Arbez M2, Brennan S3, Rafailovich M4, Hyder L4, Travlou O5, Papadakis E6, Manco-Johnson MJ7, Henschen A8, Scharrer I9.
• Thrombosis research.Thromb Res.2014 Jun;133(6):1115-23. doi: 10.1016/j.thromres.2014.03.026. Epub 2014 Mar 11.
• INTRODUCTION: Thromboelastography (TEG), a widely used clinical point of care coagulation test, is poorly understood. To investigate its fibrin determinants we used normal and variant fibrinogen isolates.MATERIALS AND METHODS: We focused mainly on the TEG maximum signal amplitude (MA), a shear modul
• PMID 24679643

Japanese Journal

• フィブリノゲン異常症合併妊娠の1例

• 神奈川産科婦人科学会誌 = Kanagawa journal of obstetrics and gynecology : official journal, Kanagawa Society of Obstetrics and Gynecology 51(2), 194-197, 2015-02
• NAID 40020386686

• 先天性低フィブリノゲン血症が疑われた犬の1例

• 動物臨床医学 23(4), 166-169, 2014
• NAID 130005125187

• 慢性骨髄性白血病の発症で偶発的に発見された先天性フィブリノゲン異常症

• 臨床血液 55(5), 541-545, 2014
• NAID 130004501848

Related Links

• Dysfibrinogenemia: Background, Pathophysiology, Epidemiology

Congenital dysfibrinogenemia is a term used to describe a relatively rare condition wherein an inherited abnormality in the fibrin molecule results in defective fibrin clot formation. The complications associated with ...

• Congenital dysfibrinogenemia: fibrinogen detroit

A 17 yr old female with a congenital bleeding disorder was found to suffer from dysfibrinogenemia. Whole blood and plasma coagulation times were delayed and thrombelastograms were grossly abnormal. Clottability of plasma ...

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★リンクテーブル★

リンク元	「先天性異常フィブリノゲン血症」
関連記事	「congenita」「congenital」「dysfibrinogenemia」

「先天性異常フィブリノゲン血症」

　　[★]

英

congenital dysfibrinogenemia

「congenita」

　　[★]

• adj.

• (後置するラテン語形容詞)先天性の

関

congenital、congenitally

• ex.

• dyskeratosis congenita、myotonia congenita

「congenital」

　　[★]

• adj.

• 生まれつきの、先天的な

　 　

「dysfibrinogenemia」

　　[★] 異常フィブリノゲン血症