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ultrasound diagnosis of fatal anomalies

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THE HEART

Fig. 5.9 Atrioventricular septal defect. Demonstration

of blood flow over the defective AV valve

using color flow mapping as well as pulsed Doppler

sonography.

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References

Achiron R, Rotstein Z, Lipitz S, Mashiach S, Hegesh J.

First-trimester diagnosis of fetal congenital heart

disease by transvaginal ultrasonography. Obstet Gynecol

1994; 84: 69–72.

Allan LD, Anderson RH, Cook AC. Atresia or absence of

the left-sided atrioventricular connection in the

fetus: echocardiographic diagnosis and outcome. Ultrasound

Obstet Gynecol 1996; 8: 295–302.

Areias JC, Matias A, Montenegro N, Brandao O. Early antenatal

diagnosis of cardiac defects using transvaginal

Doppler ultrasound: new perspectives? Diagn

Ther 1998; 13: 111–14.

Benacerraf BR, Gelman R, Frigoletto FDJ. Sonographic

identification of second-trimester fetuses with

Down’s syndrome. N Engl J Med 1987; 1371–6.

Feldt RH, Porter CJ, Edwards WD, Puga FJ, Seward JB. Atrioventricular

septal defects. In: In: Emmanouilides

GC, Allen HD, Riemenschneider TA, Gutgesell HP, editors.

Moss and Adams heart disease in infants, child-

Bradycardia

Definition: Heart frequency below 100 beats per

minute.

Incidence: One in 20 000 births.

Clinical history/genetics: 50% of cases are due to

a complete AV block resulting from an autoimmune

disease. The rate of recurrence is 8% if one

child is affected.

Teratogens: Not known.

Embryology: Autoantibodies can disturb the

cardiac stimulus conduction system. If structural

ren, and adolescents, including the fetus and young

adult. Baltimore: Williams & Wilkins, 1995: 704–24.

Murphy DJ Jr. Atrioventricular canal defects. Curr Treat

Options Cardiovasc Med 1999; 1: 323–34.

Paladini D, Calabrb R, Palmieri S, Dandrea T. Prenatal diagnosis

of congenital heart disease and fetal karyotyping.

Obstet Gynecol 1993; 81: 679–82.

Park JK, Taylor DK, Skeels M, Towner DR. Dilated coronary

sinus in the fetus: misinterpretation as an atrioventricular

canal defect. Ultrasound Obstet Gynecol

1997; 10: 126–9.

Stoll C, Dott B, Alembik Y, Roth MP. Evaluation of routine

prenatal ultrasound examination in detecting fetal

chromosomal abnormalities in a low risk population.

Hum Genet 1993; 91: 37–41.

Tennstedt C, Chaoui R, Korner H, Dietel M. Spectrum of

congenital heart defects and extracardiac malformations

associated with chromosomal abnormalities:

results of a seven year necropsy study. Heart 1999;

82: 34–9.

malformation is the cause, then the atrioventricular

septum is mostly involved.

Associated malformations: In 50% of cases, complex

cardiac anomalies are present such as AV

canal, VSD, atrial isomerism, or abnormal

venous flow. Fetal hydrops must be excluded. If

there is sinus bradycardia, malformation of the

central nervous system and fetal growth restriction

should be looked for.

Ultrasound findings: A very slow heartbeat is the

first sign detected in B-mode. M-mode echocardiography

is needed for further differentiation.

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