WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
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
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- 1. 脾腫およびその他の脾疾患を有する成人患者に対するアプローチ approach to the adult patient with splenomegaly and other splenic disorders
- 2. 無脾症患者における敗血症の予防 prevention of sepsis in the asplenic patient
- 3. 無脾症患者における敗血症の臨床的特徴およびマネージメント clinical features and management of sepsis in the asplenic patient
- 4. 好中球増多症の原因 causes of neutrophilia
- 5. 鎌状赤血球症を有する小児に対する定期的な包括的ケア routine comprehensive care for children with sickle cell disease
English Journal
- Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
- Saunders CJ, Miller NA, Soden SE, Dinwiddie DL, Noll A, Alnadi NA, Andraws N, Patterson ML, Krivohlavek LA, Fellis J, Humphray S, Saffrey P, Kingsbury Z, Weir JC, Betley J, Grocock RJ, Margulies EH, Farrow EG, Artman M, Safina NP, Petrikin JE, Hall KP, Kingsmore SF.SourceCenter for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
- Science translational medicine.Sci Transl Med.2012 Oct 3;4(154):154ra135. doi: 10.1126/scitranslmed.3004041.
- Monogenic diseases are frequent causes of neonatal morbidity and mortality, and disease presentations are often undifferentiated at birth. More than 3500 monogenic diseases have been characterized, but clinical testing is available for only some of them and many feature clinical and genetic heteroge
- PMID 23035047
- An unusual form of supracardiac total anomalous pulmonary venous return via a right-sided vertical vein in a heterotaxy syndrome case.
- Lehner A, Kozlik-Feldmann R, Herrmann F, Dalla-Pozza R, Netz H, Malec E, Januszewska K.SourcePediatric Cardiology and Intensive Care, Ludwig-Maximilians-University, Munich, Germany, Anja.Lehner@med.uni-muenchen.de.
- Pediatric cardiology.Pediatr Cardiol.2012 Oct;33(7):1200-2. Epub 2012 Feb 22.
- Heterotaxy syndromes comprise a great variety of possible cardiac defects. Anomalies of the pulmonary venous system are well recognized in heterotaxy syndromes but constitute a frequently underdiagnosed subgroup. The case report describes a girl with a rare form of supracardiac total anomalous pulmo
- PMID 22354227
Japanese Journal
- Polysplenia or Left Isomerism?
- Internal Medicine 55(5), 555-555, 2016
- NAID 130005132636
- Case Studies of Patients Successfully and Unsuccessfully Managed Pre- and Post-Fontan Procedure
- International Heart Journal 56(Supplement), S31-S34, 2015
- NAID 130004941329
- Glenn手術後の呼吸循環管理にairway pressure release ventilation（APRV）が著効した一例
- 日本集中治療医学会雑誌 21(5), 501-505, 2014
- NAID 130004691321
Related Links
- Heterotaxy Syndrome - Types (Asplenia, Polysplenia) - Symptoms, Causes, Treatment, Life Expectancy, Prognosis, in men, women, infants and Definition... ... What is Heterotaxy Syndrome? Heterotaxy syndrome is a birth defect ...
- a·sple·ni·a syn·drome syndrome seen in patients who have no functional spleen, either because of surgical removal or disease (for example, sickle cell anemia); includes increased susceptibility to bacterial infection, especially of the ...
Related Pictures
★リンクテーブル★
| リンク元 | 「無脾症候群」「無脾症」 |
| 関連記事 | 「asplenia」「syndrome」 |
「無脾症候群」
- 英
- asplenia syndrome
- 関
- 無脾症。多脾症、多脾症候群
概念
病態
- 肺 ：両肺ともに右型
- 大血管：両側上大静脈
- 心臓：心房が右型
- 内臓
- 肝臓：対称肝
- 胃 ：胃泡は中心に認められる
検査
- 血液検査
- 末梢血塗沫：ハウエル・ジョリー小体
「無脾症」
「asplenia」
「syndrome」
- n.