- 関
- antibody deficiency syndrome
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
UpToDate Contents
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English Journal
- Cuba: defeating mother-to-child transmission of syphilis.
- Bristow CC1, Klausner JD2.
- Lancet (London, England).Lancet.2015 Oct 17;386(10003):1533. doi: 10.1016/S0140-6736(15)00485-7.
- PMID 26530617
- Chediak-Higashi syndrome: Lysosomal trafficking regulator domains regulate exocytosis of lytic granules but not cytokine secretion by natural killer cells.
- Gil-Krzewska A1, Wood SM2, Murakami Y1, Nguyen V1, Cher Chiang SC2, Cullinane AR3, Peruzzi G1, Gahl WA3, Coligan JE1, Introne WJ3, Bryceson YT2, Krzewski K4.
- The Journal of allergy and clinical immunology.J Allergy Clin Immunol.2015 Oct 15. pii: S0091-6749(15)01264-6. doi: 10.1016/j.jaci.2015.08.039. [Epub ahead of print]
- BACKGROUND: Mutations in lysosomal trafficking regulator (LYST) cause Chediak-Higashi syndrome (CHS), a rare immunodeficiency with impaired cytotoxic lymphocyte function, mainly that of natural killer (NK) cells. Our understanding of NK cell function deficiency in patients with CHS and how LYST regu
- PMID 26478006
- Severe epistaxis due to aberrant vasculature in a patient with STAT-1 mutation.
- Chang MT1, Schwam ZG1, Hajek MA1, Paskhover B1, Judson BL1.
- Head & neck.Head Neck.2015 Oct 7. doi: 10.1002/hed.24165. [Epub ahead of print]
- BACKGROUND: Signal transducer and activator 1 (STAT-1) mutations are rare and have been implicated in combined immunodeficiency, enhanced tumorigenesis, and vascular defects.METHODS: A 60-year-old woman with a novel STAT-1 mutation and resulting immunodeficiency, squamous cell carcinoma, and vascula
- PMID 26445901
Japanese Journal
- ITPに合併した抗VWF抗体によるvon Willebrand症候群
- 井原 章裕,鈴木 伸明,松下 正 [他],一瀬 白帝
- 臨床血液 56(7), 901-904, 2015
- … 後天性von Willebrand syndrome(以下AVWS)は,先天性VWD類似の稀な疾患である。 …
- NAID 130005093126
- Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to activation-induced cytidine deaminase deficiency
- 悪性貧血患者に発症したインフルエンザウイルス関連血球どん食症候群
- 城野 憲二,津田 弘之,赤星 泉
- 臨床血液 37(6), 511-513, 1996
- … A 59-year-old man with pernicious anemia (vitamin B12 deficiency) was admitted because of rapidly developing pancytopenia with the symptoms of influenza. … Laboratory data indicated that the pancytopenia was manifested by influenza virus-associated hemophagocytic syndrome. … In the patients with pernicious anemia, it is known that there are immunologic disturbances in either humoral and cellular immunity and increased hematopoiesis due to ineffective hematopoiesis. …
- NAID 130004500273
Related Links
- Definition of Immunologic deficiency syndromes in the Medical Dictionary. Immunologic deficiency syndromes explanation. Information about Immunologic deficiency syndromes in Free online English dictionary. What is Bing ...
- DiGeorge syndrome Definition DiGeorge syndrome is a rare congenital disease that affects an infant's immune system and that is due to a large deletion from chromosome 22. The syndrome is marked by absence or ...
Related Pictures
★リンクテーブル★
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抗体不全症候群
- 関
- immunologic deficiency syndrome
[★]
- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
[★]
- 関
- immune
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