congenital cardiovascular anomalies
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/1/1/2/3/3/656ea7cc270fb78cea3b7e96b0b83a_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/1/1/2/3/7/4175c6fedcadd8259b809ed0c07fbb_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/0/2/6/7/6/af7a0a1afd24a36b31e4a24bb04b09_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/0/2/6/6/2/2397504f7c944b7a70cc749674a712_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/0/2/7/1/1/4ac4a54b9f51092b7e4e441f4db3df_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/0/2/8/2/2/6d94534b9491028d4f6ce2d48d58ee_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/0/2/6/7/3/8b7c93613763fc37070b6fad2f379e_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/1/1/2/4/7/ANNOTATED_A_big_gallery_thumb.jpg)
![](https://pacs.de/sites/default/files/pictures/thumbs/data.pacs.de/1/0/2/6/6/0/09247062115ef458e7c98433d0330b_big_gallery_thumb.jpg)
Congenital cardiovascular anomalies are relatively common, with an incidence of up to 1% if small muscular VSDs are included. As a group, there is a much greater frequency in syndromic infants and in those that are stillborn.
Clinical presentation
Broadly, congenital cardiovascular anomalies can be clinically divided into:
Depending on the lesion and its severity, patients may be asymptomatic or conversely, may present with rapidly deteriorating congestive cardiac failure.
Pathology
These defects as a group have a heterogeneous etiology with many resulting from an interplay between both genetic and environmental factors.
Subtypes
A list of anomalies and their approximate occurrences (as a percentage of all congenital cardiac disease) are given below:
- ventricular septal defect (VSD): 40%
- atrial septal defect (ASD): 10%
- congenital pulmonary stenosis: 8%
- patent ductus arteriosus (PDA): 7%
- transposition of the great arteries (TGA): 7%
- tetralogy of Fallot (TOF): 5%
- coarctation of the aorta: 5%
- atrioventricular septal defect (AVSD): 4%
- congenital aortic stenosis: 4%
- hypoplastic left heart syndrome (HLHS): 4%
- double outlet right ventricle (DORV): 2%
- interrupted aortic arch (IAA): 1.5%
- truncus arteriosus: 1%
- total anomalous pulmonary venous return (TAPVR): 1%
- tricuspid atresia: 1%
- pulmonary atresia:
- Ebstein anomaly: 0.7%
- Bland-White-Garland syndrome: ~0.5%
- cor triatriatum: ~0.1%
- partial anomalous pulmonary venous return (PAPVR): 0.5%
- double outlet left ventricle (DOLV)
- aortopulmonary septal defect: <1%
- Gerbode defect: <1%
- Shone complex: <1%
- hypoplastic right heart syndrome (HRHS)
- aortoventricular tunnel <0.1%
Other valvular anomalies
Percentages may not necessarily add up to 100 due to overlap and simultaneous occurrence of abnormalities.
Associations
Congenital cardiac anomalies can be found with many aneuploid conditions which include:
- trisomy 18: up to 90% can have cardiac anomalies
- trisomy 13: up to 90%
- trisomy 21: up to 50%
- Turner syndrome: up to 40%
Siehe auch:
- Chiari-Netz
- Aortenisthmusstenose
- Pätau-Syndrom
- Persistierender Ductus arteriosus
- Atriumseptumdefekt
- Down-Syndrom
- Ebstein anomaly
- Cor triatriatum
- Normvarianten Koronararterien
- Varianten der Herzanatomie
- Trisomie 18
- Turner-Syndrom
- tricuspid atresia
- Fallot'sche Tetralogie
- hypoplastic left heart syndrome
- Transposition der großen Arterien
- quadricuspid aortic valve
- Bikuspidalität der Aortenklappe
- Bland-White-Garland-Syndrom
- Divertikel des linken Vorhofs
- double outlet right ventricle (DORV)
- congenital aortic stenosis
- conotruncal cardiac anomalies
- atrioventricular septal defect (AVSD)
- Single Ventricle
- totale Lungenvenenfehlmündung
- Pulmonalatresie
- Normale Herzkonfiguration im Röntgen-Thorax
- Valvula Eustachii
- partielle Lungenvenenfehlmündung
- Ventrikelseptumdefekt
- Truncus arteriosus communis
- fibromuskuläres Band im linken Vorhof
- congenital heart disease : CXR approach
- Atresie der Aorta
- kongenitale Pulmonalstenose
und weiter:
- Ektasie Aorta ascendens
- einseitig vermehrte Transparenz Thorax
- Situs inversus
- Lungensequester
- obstetric curriculum
- Ösophagusatresie
- Herzfehler
- Chylothorax
- Hydrops fetalis
- Kardiomegalie
- acute respiratory distress syndrome (ARDS)
- Ellis-van-Creveld-Syndrom
- mandibuläre Retrognathie
- acyanotic congenital heart disease
- Mikrognathie
- Situs ambiguus
- rechts descendierende Aorta
- fetal conditions associated with maternal diabetes
- Fetales Valproat-Syndrom
- nuchal translucency
- Diastrophische Dysplasie
- fetal pleural effusion
- Abernethy malformation
- CXR approach to congenital heart disease
- Surfactant-Mangelsyndrom
- caudal dysplasia sequence
- CHARGE-Syndrom
- abnormal ductus venosus waveforms
- Embryopathia rubeolosa
- chest x-ray appeoach to congenital heart disease
- Cornelia-de-Lange-Syndrom
- polysplenia
- Lungensequester extralobulär
- congenital heart disease - chest x-ray approach
- nuchal thickness
- mesoectodermal dysplasia
- Herz Anatomie
- Rubinstein-Taybi-Syndrom
- Fryns-Syndrom
- Goldenhar-Gorlin-Syndrom
- Golfballphänomen
- fetal complete atrioventricular block
- Kabuki-Syndrom
- fetal tachyarrhythmia
- camptomelic dysplasia
- hydrolethalus
- endocardial cushion defect
- kongenitale pulmonale Atemwegsmalformation (CPAM)
- McKusick-Kaufman-Syndrom
- anomalous left coronary artery off the pulmonary artery
- dilantin embryopathy
- absent ductus venosus
- verzögerte Skelettreifung
- four chamber cardiac view
- fetal bradyarrhythmia
- epikardiale Schrittmachersonden
- congenital vascular anomalies
- transient tachypnea of newborn
- iron deficiency anaemia
- camptomelic dwarfism
- lentiginosis profusa syndrome
- fetal premature atrial contractions
- fetal nuchal oedema
- retained foetal fluid
- cyanotic congenital cardiac anomaly
- Zyanotischer Herzfehler
- Thrombozytopenie-Radiusaplasie-Syndrom
- Valvula thebesii
- Membran im linken Vorhof
- Zephalozele
- double chamber right ventricle (DCRV)
- Herzektopie
- Miller-Dieker Syndrom
- Nabelvenenaneurysma
- kongenitaler Hydrozephalus
![Click für weniger anzeigen](/sites/all/modules/pacs/tools/imgs/collapse_up.png)
![](/sites/all/modules/pacs/tools/imgs/Iris_color_40.png)