WordNet
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
- abnormal narrowing of a bodily canal or passageway (同)stricture
PrepTutorEJDIC
- (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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- 1. 小児における大動脈弁狭窄 valvar aortic stenosis in children
- 2. 成人における大動脈二尖弁の臨床症状および診断 clinical manifestations and diagnosis of bicuspid aortic valve in adults
- 3. 大動脈弁上狭窄 supravalvar aortic stenosis
- 4. 大動脈弁下狭窄（大動脈弁下部狭窄） subvalvar aortic stenosis subaortic stenosis
- 5. 成人における大動脈二尖弁疾患のマネージメント management of adults with bicuspid aortic valve disease
English Journal
- Successful introduction of interventional catheterisation and other paediatric cardiology services in a developing country.
- Tomita H, Haneda N, Higaki T, Kataoka K.Source1 Cardiovascular Center, Showa University Northern Yokohama Hospital, Yokohama, Kanagawa, Japan.
- Cardiology in the young.Cardiol Young.2013 Jun;23(3):405-8. doi: 10.1017/S104795111200100X. Epub 2012 Aug 22.
- BACKGROUND: Providing care for children with cardiac disease remains a challenge in developing countries. Materials and methods Since 2001, a team of paediatric cardiologists has been visiting Mongolia to perform children's cardiac catheterisation, as well as screening children for cardiac disease.
- PMID 22914368
- Repair of anomalous origin of the left coronary artery from the pulmonary artery in infants.
- Kazmierczak PA, Ostrowska K, Dryzek P, Moll JA, Moll JJ.SourceDepartment of Cardiosurgery, Polish Mother's Memorial Hospital-Research Institute, Lodz, Poland.
- Interactive cardiovascular and thoracic surgery.Interact Cardiovasc Thorac Surg.2013 Jun;16(6):797-801. doi: 10.1093/icvts/ivt061. Epub 2013 Feb 26.
- OBJECTIVES Anatomical repair seems an ideal method for the surgical treatment of the anomalous left coronary artery arising from the pulmonary artery (ALCAPA) in infancy. The medium-term outcome has been investigated for infants with ALCAPA following the restoration of a dual-coronary arterial circu
- PMID 23442939
Japanese Journal
- Patch annulo-aortoplasty in an adult patient with congenital supravalvular aortic stenosis and a small aortic annulus
- MORIMOTO Naoto,MORIMOTO Keisuke,MORIMOTO Yoshihisa,TANAKA Akiko,SAKAMOTO Toshihito,OKADA Kenji,OKITA Yutaka
- General thoracic and cardiovascular surgery 59(8), 569-571, 2011-08-10
- NAID 10029827103
- 短絡のない非チアノーゼ性心疾患 (特集 胸部外科診療に役立つ疾患別最新データ) -- (心臓血管領域)
- 新保 秀人
- 胸部外科 64(8), 673-678, 2011-07
- NAID 40018928798
Related Links
- Aortic stenosis is a heart defect that may be congenital (present at birth) or acquired (develop later in life). If the problem is congenital, then something occurred during the first 8 weeks of pregnancy to affect the development of the aortic valve.
- Aortic stenosis is most commonly caused by age-related progressive calcification of a normal (three-leafed) aortic valve (>50% of cases) mean age 65 to 70 years old - most common cause. Other causes include calcification of a congenital ...
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★リンクテーブル★
| リンク元 | 「先天性大動脈狭窄」「先天性大動脈狭窄症」 |
| 関連記事 | 「congenita」「aortic」「aortic stenosis」「congenital」 |
「先天性大動脈狭窄」
「先天性大動脈狭窄症」
「congenita」
- adj.
- (後置するラテン語形容詞)先天性の
- ex.
「aortic」
- adj.
- 大動脈の
「aortic stenosis」
「congenital」
- adj.
- 生まれつきの、先天的な