WordNet
- United States geneticist who (with Crick in 1953) helped discover the helical structure of DNA (born in 1928) (同)James Watson, James Dewey Watson
- United States psychologist considered the founder of behavioristic psychology (1878-1958) (同)John Broadus Watson
- United States telephone engineer who assisted Alexander Graham Bell in his experiments (1854-1934) (同)Thomas Augustus Watson
- 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. 新生児胆汁うっ滞の原因 causes of neonatal cholestasis
- 2. 抱合型高ビリルビン血症関連の遺伝性疾患 inherited disorders associated with conjugated hyperbilirubinemia
- 3. 微細欠失症候群（12番～22番染色体） microdeletion syndromes chromosomes 12 to 22
- 4. 小児における胆道疾患のERCP ercp for biliary disease in children
- 5. 新生児、乳児、および小児における肺動脈狭窄（PS） pulmonic stenosis ps in neonates infants and children
English Journal
- A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings.
- Wallis MJ1,2, Kelly AL1, Peters GB3, St Heaps L3, Nandini A4, McGaughran JM1,2.
- American journal of medical genetics. Part A.Am J Med Genet A.2016 Jul;170(7):1930-3. doi: 10.1002/ajmg.a.37689. Epub 2016 May 9.
- PMID 27159256
- CT-defined phenotype of pulmonary artery stenoses in Alagille syndrome.
- Rodriguez RM1, Feinstein JA2,3, Chan FP4.
- Pediatric radiology.Pediatr Radiol.2016 Jul;46(8):1120-7. doi: 10.1007/s00247-016-3580-4. Epub 2016 Apr 4.
- BACKGROUND: Alagille syndrome is a rare disorder commonly associated with pulmonary artery stenosis. Studies exist discussing the cardiovascular sequela but no consistent phenotype, or pattern of pulmonary artery stenosis, has been described.OBJECTIVE: The objective of this study was to characterize
- PMID 27041277
- Focal liver hyperplasia in a patient with Alagille syndrome: Diagnostic difficulties. A case report.
- Ennaifer R1, Ben Farhat L2, Cheikh M3, Romdhane H3, Marzouk I2, Belhadj N3.
- International journal of surgery case reports.Int J Surg Case Rep.2016 Jun 4;25:55-61. doi: 10.1016/j.ijscr.2016.03.032. [Epub ahead of print]
- INTRODUCTION: Alagille syndrome is a multisystem autosomal disorder. The main clinical features are chronic cholestasis due to paucity of intrahepatic bile ducts, which can progress to cirrhosis and liver failure.PRESENTATION OF CASE: A 15 year-old girl with Alagille syndrome was referred for liver
- PMID 27322896
Related Links
- syndrome /syn·drome/ (sin´drōm) a set of symptoms occurring together; the sum of signs of any morbid state; a symptom complex. See also entries under disease. Aarskog syndrome , Aarskog-Scott syndrome a hereditary X-linked ...
- Watson Alagille syndrome symptoms, causes, diagnosis, and treatment information for Watson Alagille syndrome (Alagille Syndrome) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention ...
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★リンクテーブル★
| リンク元 | 「ワトソン・アラジール症候群」 |
| 関連記事 | 「Alagille syndrome」「syndrome」 |
「ワトソン・アラジール症候群」
「Alagille syndrome」
「syndrome」
- n.