congenital cardiac anomalies
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:
- Aortenisthmusstenose
- Chiari-Netz
- Pätau-Syndrom
- Persistierender Ductus arteriosus
- Atriumseptumdefekt
- Normvarianten Koronararterien
- Down-Syndrom
- Ebstein anomaly
- Cor triatriatum
- Turner-Syndrom
- Fallot'sche Tetralogie
- Trisomie 18
- tricuspid atresia
- Transposition der großen Arterien
- hypoplastic left heart syndrome
- Bland-White-Garland-Syndrom
- Bikuspidalität der Aortenklappe
- quadricuspid aortic valve
- double outlet right ventricle (DORV)
- Divertikel des linken Vorhofs
- atrioventricular septal defect (AVSD)
- conotruncal cardiac anomalies
- congenital aortic stenosis
- totale Lungenvenenfehlmündung
- Pulmonalatresie
- partielle Lungenvenenfehlmündung
- Normale Herzkonfiguration im Röntgen-Thorax
- Single Ventricle
- Ventrikelseptumdefekt
- Valvula Eustachii
- Valvula thebesii
- Varianten linkes Herzohr
- fibromuskuläres Band im linken Vorhof
- Truncus arteriosus communis
- congenital heart disease : CXR approach
- kongenitale Pulmonalstenose
- Atresie der Aorta
und weiter:
- Ektasie Aorta ascendens
- einseitig vermehrte Transparenz Thorax
- Lungensequester
- Situs inversus
- obstetric curriculum
- acute respiratory distress syndrome (ARDS)
- Herzfehler
- Ösophagusatresie
- Kardiomegalie
- Chylothorax
- Hydrops fetalis
- mandibuläre Retrognathie
- acyanotic congenital heart disease
- rechts descendierende Aorta
- Situs ambiguus
- Mikrognathie
- Ellis-van-Creveld-Syndrom
- fetal conditions associated with maternal diabetes
- nuchal translucency
- Diastrophische Dysplasie
- kongenitale pulmonale Atemwegsmalformation (CPAM)
- Fetales Valproat-Syndrom
- fetal pleural effusion
- CXR approach to congenital heart disease
- caudal dysplasia sequence
- abnormal ductus venosus waveforms
- Embryopathia rubeolosa
- Abernethy malformation
- Golfballphänomen
- CHARGE-Syndrom
- nuchal thickness
- Surfactant-Mangelsyndrom
- Rubinstein-Taybi-Syndrom
- Cornelia-de-Lange-Syndrom
- chest x-ray appeoach to congenital heart disease
- Herz Anatomie
- epikardiale Schrittmachersonden
- Goldenhar-Gorlin-Syndrom
- congenital heart disease - chest x-ray approach
- Fryns-Syndrom
- endocardial cushion defect
- Lungensequester extralobulär
- mesoectodermal dysplasia
- Kabuki-Syndrom
- fetal complete atrioventricular block
- fetal tachyarrhythmia
- camptomelic dysplasia
- verzögerte Skelettreifung
- dilantin embryopathy
- anomalous left coronary artery off the pulmonary artery
- hydrolethalus
- absent ductus venosus
- McKusick-Kaufman-Syndrom
- Thrombozytopenie-Radiusaplasie-Syndrom
- four chamber cardiac view
- transient tachypnea of newborn
- congenital vascular anomalies
- fetal bradyarrhythmia
- lentiginosis profusa syndrome
- Zyanotischer Herzfehler
- iron deficiency anaemia
- fetal premature atrial contractions
- Polysplenie-Syndrom
- camptomelic dwarfism
- fetal nuchal oedema
- retained foetal fluid
- cyanotic congenital cardiac anomaly
- Zephalozele
- Membran im linken Vorhof
- Miller-Dieker Syndrom
- Herzektopie
- double chamber right ventricle (DCRV)
- Nabelvenenaneurysma
- kongenitaler Hydrozephalus
