WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- the 9th letter of the Roman alphabet (同)i
- publicize in an exaggerated and often misleading manner
- immunological disorder in which some part of the bodys immune system is inadequate and resistance to infectious diseases is reduced
PrepTutorEJDIC
- (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
- 『私は』私が
- iodineの化学記号
- …‘を'刺激する,駆り立てる / (不正な手段で)〈評判など〉‘を'高める,強化する / 不正な手段 / (皮下注射による)麻薬中毒者
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 原発性の体液性免疫不全：概要 primary humoral immune deficiencies an overview
- 2. 高IgM症候群 hyperimmunoglobulin m syndromes
- 3. 複合免疫不全 combined immunodeficiencies
- 4. 成人における分類不能型免疫不全の臨床症状、疫学、および診断 clinical manifestations epidemiology and diagnosis of common variable immunodeficiency in adults
- 5. 小児における分類不能型免疫不全症 common variable immunodeficiency in children
English Journal
- Molecular diagnostic challenges and complex management of consecutive twin pregnancies in a family with CD40 ligand deficiency.
- Torok O, Toth B, Erd?s M, Csorba G, Gyimesi E, Balogh I, Toth Z, Marodi L.SourceDepartments of Obstetrics and Gynecology Infectious and Pediatric Immunology Internal Medicine Laboratory Medicine, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary.
- Scandinavian journal of immunology.Scand J Immunol.2011 Sep 29. doi: 10.1111/j.1365-3083.2011.02644.x. [Epub ahead of print]
- X-linked hyper-IgM syndrome (XHIGM) is a primary immunodeficiency disorder caused by mutation in the gene encoding the CD40 ligand (CD40L) expressed on activated T cells. Prenatal genotyping in carriers with twin pregnancies is more challenging than in women with single pregnancies. In addition, wom
- PMID 21958324
- Cutaneous Manifestations of DOCK8 Deficiency Syndrome.
- Chu EY, Freeman AF, Jing H, Cowen EW, Davis J, Su HC, Holland SM, Turner ML.SourceCenter for Cancer Research, National Cancer Institute (Drs Chu, Cowen, and Turner), and the National Institute of Allergy and Infectious Diseases (Drs Freeman, Jing, Su, and Holland and Ms Davis), Bethesda, Maryland. Dr Chu is now with the Department of Dermatology, Hospital of the University of Pennsylvania, Philadelphia.
- Archives of dermatology.Arch Dermatol.2011 Sep 19. [Epub ahead of print]
- BACKGROUND: Mutations in the dedicator of cytokinesis 8 gene (DOCK8) cause a combined primary immunodeficiency syndrome that is characterized by elevated serum IgE levels, depressed IgM levels, eosinophilia, sinopulmonary infections, cutaneous viral infections, and lymphopenia. Many patients with DO
- PMID 21931011
Japanese Journal
- Progressive Multifocal Leukoencephalopathy Complicating X-linked Hyper-IgM Syndrome in an Adult
- Suzuki Hitoshi,Takahashi Yoshitomo,Miyajima Hiroaki
- Internal Medicine 45(20), 1187-1188, 2006
- NAID 130000076639
- An Adult Diagnosed as Hyper-IgM Immunodeficiency Syndrome
- HIRASAWA Akira,SATO Tabatsugu,NISHIKAWA Tetsuo,UOZUMI Kimiharu,WAKABAYASHI Yoshihisa,TAKEUCHI Kouichirou,CHIBA Shyozo
- Internal medicine 34(7), 640-642, 1995-07
- … A 27-year-old male who visited our hospital because of pneumonia was diagnosed as hyper-IgM immunodeficiency syndrome. … His serum IgM level was markedly elevated, while the serum level of IgD was normal with a markedly decreased level of serum IgG and IgA. …
- NAID 10006168609
Related Links
- 28 Sep 2010 ... X-linked immunodeficiency with hyper?immunoglobulin M (XHIGM or HIGM1) is a rare form of primary immunodeficiency disease caused by mutations in the gene that codes for CD40 ligand (CD40L, also known as CD154 ...
Related Pictures
★リンクテーブル★
| リンク元 | 「高IgM免疫不全症候群」 |
| 拡張検索 | 「type 1 hyper-IgM immunodeficiency syndrome」 |
| 関連記事 | 「I」「IgM」「hyper」「immunodeficiency」「Ig」 |
「高IgM免疫不全症候群」
「type 1 hyper-IgM immunodeficiency syndrome」
「I」
「IgM」
臨床関連
増加
「hyper」
- comb form.