WordNet

deviation from the normal or common order or form or rule (同)anomalousness
a person who is unusual (同)unusual person
(astronomy) position of a planet as defined by its angular distance from its perihelion (as observed from the sun)
of or pertaining to or involving the heart and blood vessels; "cardiovascular conditioning"
present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate

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1. 重症先天性心疾患を有する新生児の識別 identifying newborns with critical congenital heart disease
2. 先天性および小児冠動脈異常 congenital and pediatric coronary artery abnormalities
3. 先天性心疾患女性における妊娠：特定病変 pregnancy in women with congenital heart disease specific lesions
4. 三尖弁のエプスタイン奇形 ebsteins anomaly of the tricuspid valve
5. 心血管MRIの臨床的有用性 clinical utility of cardiovascular magnetic resonance imaging

Congenital coronary artery anomalies in adults: review of 111 cases from a single-centre experience.

Çanga Y1, Güvenç TS1, Karataş MB1, Çalık AN1, Onuk T1, Tanık VO1, Güngör B1, Bolca O1.
Cardiology in the young.Cardiol Young.2016 Nov 15:1-10. [Epub ahead of print]
BACKGROUND: Coronary artery anomalies are a heterogeneous group of congenital disorders presenting with a wide spectrum of symptoms, ranging from vague chest pain to sudden cardiac death. Despite available data, there is no consensus about the classification, nomenclature, and outcomes of coronary a
PMID 27842619

Repair of anomalous coronary artery from the pulmonary artery: A-signal center 20-year experience.

Qiu J1, Li S1, Yan J1, Wang Q1, Song Y1, Sun H1, Li D2.
International journal of cardiology.Int J Cardiol.2016 Nov 15;223:625-629. doi: 10.1016/j.ijcard.2016.08.221. Epub 2016 Aug 13.
BACKGROUND: Anomalous origin of coronary artery from the pulmonary artery (ACAPA) is a rare congenital coronary malformation with a high mortality whether in infants or adult patients. This study reviews 20years of surgical treatment in a single center and aims to establish the optimal surgical stra
PMID 27565839

Muntean I1, Togănel R2, Benedek T3.
Biochemical genetics.Biochem Genet.2016 Nov 2. [Epub ahead of print]
Congenital heart disease is the most common congenital anomaly, representing an important cause of infant morbidity and mortality. Congenital heart disease represents a group of heart anomalies that include septal defects, valve defects, and outflow tract anomalies. The exact genetic, epigenetic, or
PMID 27807680

Open Surgical Repair for a Ruptured Abdominal Aortic Aneurysm with a Horseshoe Kidney

先天性心疾患.xls

参考文献(2)より

心疾患による症状
	肺血流増加	肺血流減少	低心拍出
1．新生児期・乳児早期	多呼吸，陥没呼吸，呼吸困難，喘鳴，多汗，哺乳障害	チアノーゼ	蒼白，末梢冷感，冷汗，網状チアノーゼ，体重増加不良，弱い泣き声
2．乳幼児期	多呼吸，易感染性，反復する肺炎	チアノーゼ，低酸素発作，蹲踞	体重増加不良，運動発達遅延，易疲労性，顔色不良，やせ
3．小児期	運動能低下，息切れ	ばち状指	運動能低下，動悸
4．思春期以後　合併症による症状	胸痛，失神発作，突然死，喀血，不整脈，出血傾向，痛風，けいれん　等

大動脈縮窄・大動脈離断、大動脈閉鎖

心室中隔欠損、大動脈縮窄複合、完全心内膜床欠損、総動脈幹遺残、

完全大血管転位（II型）、三尖弁閉鎖（C型）、大動脈肺動脈窓など

QB.C-478

疾患	先天性心奇形	その他
22q11.2欠失症候群	ファロー四徴症、総動脈幹症(truncus arteriosus)、心室中隔欠損を伴う肺動脈弁閉鎖症、大動脈弓離断、右側大動脈弓、右側肺動脈の大動脈起始	胸腺低形成、低カルシウム血症、特有の顔貌、口蓋裂
ダウン症候群	(50%の例に合併)。心房中隔欠損症(ASD), 心室中隔欠損症(VSD)
先天性風疹症候群	心房中隔欠損症、動脈管開存症、末梢肺動脈狭窄
ターナー症候群	大動脈縮窄症	低身長・翼状頚、外反肘
ヌーナン症候群	肺動脈弁狭窄、肥大型心筋症	ターナー症候群に似る
マルファン症候群	僧帽弁逸脱症、大動脈弁閉鎖不全症
糖代謝異常合併妊娠母体からの出生児	大血管転位症
ウイリアムズ症候群	大動脈弁上狭窄、末梢肺動脈狭窄
無脾症、多脾症	単心房、単心室、総肺静脈還流異常