多発性先天異常
WordNet
- having or involving or consisting of more than one part or entity or individual; "multiple birth"; "multiple ownership"; "made multiple copies of the speech"; "his multiple achievements in public life"; "her multiple personalities"; "a pineapple is a multiple fruit"
- the product of a quantity by an integer; "36 is a multiple of 9"
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
PrepTutorEJDIC
- 多数の部分(要素)から成る,複合の,複式の / 倍数
- (病気・身体的欠陥など)生まれつきの,先天的な
UpToDate Contents
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English Journal
- The concept of double inlet-double outlet right ventricle: a distinct congenital heart disease.
- Spadotto V1, Frescura C1, Ho SY2, Thiene G3.
- Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.Cardiovasc Pathol.2017 Jan - Feb;26:39-44. doi: 10.1016/j.carpath.2016.09.003. Epub 2016 Sep 25.
- The aim of this study was to estimate the incidence and to analyze the anatomy of double inlet-double outlet right ventricle complex and its associated cardiac anomalies in our autopsy series. Among the 1640 hearts with congenital heart disease of our Anatomical Collection, we reviewed the specimens
- PMID 27866077
- Genetic determinants of myocardial dysfunction.
- Li X1,2,3,4, Zhang P1,2,3,4.
- Journal of medical genetics.J Med Genet.2017 Jan;54(1):1-10. doi: 10.1136/jmedgenet-2016-104308. Epub 2016 Nov 21.
- Heart failure (HF) is a major killer with high morbidity and mortality and nearly 37.7 million people are affected by HF globally, making this a global epidemic. HF is a complex pathophysiological syndrome in which the mechanical function of heart for pumping blood is compromised. Cardiac structural
- PMID 27872154
- Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects.
- Cowan JR1,2, Tariq M2,3, Shaw C4, Rao M4, Belmont JW4, Lalani SR4, Smolarek TA5, Ware SM6.
- Philosophical transactions of the Royal Society of London. Series B, Biological sciences.Philos Trans R Soc Lond B Biol Sci.2016 Dec 19;371(1710). pii: 20150406.
- Genomic disorders and rare copy number abnormalities are identified in 15-25% of patients with syndromic conditions, but their prevalence in individuals with isolated birth defects is less clear. A spectrum of congenital heart defects (CHDs) is seen in heterotaxy, a highly heritable and genetically
- PMID 27821535
Japanese Journal
- 発達により ABR が正常化した Cornelia de Lange 症候群の一例
- 多発性硬化症の妊娠・出産-自験例を含めた最近の知見-
Related Links
- When a patient has multiple abnormalities (multiple anomaly, multiple deformity), they have a congenital abnormality that can not be primarily identified with a single system of the body or single disease process. Most medical conditions can ...
- Genetic Services Policy Project. Multiple Congenital Anomalies. What are multiple congenital anomalies (MCA)? Infants with multiple congenital anomalies (MCA) are typically infants with: • two or more major malformations (e.g., a neural tube ...
★リンクテーブル★
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- 英
- multiple congenital abnormalities
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- 関
- congenital、congenitally
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- 関
- multifocality、multiplex、plural
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