To determine the developmental changes in the myocardial current during fetal life, and to evaluate the clinical usefulness of magnetocardiography for prenatal diagnosis of cardiac hypertrophy or enlargement, we approximated the magnitude of the one-current dipole of the fetal heart using fetal magnetocardiography (fMCG). A total of 95 fetuses with gestational age of 20 -40 wk were included in this study. fMCG was recorded with a nine-channel superconducting quantum interference device system in a magnetically shielded room. The magnitude of the dipole (Q) was calculated using an equation based on the fMCG amplitude obtained on the maternal abdomen and the distance between the maternal surface and fetal heart measured ultrasonographically. In uncomplicated pregnancies, the Q value correlated significantly with gestational age, reflecting an increase in the amount of myocardial current, i.e. myocardial mass. Moreover, the Q values in fetuses with cardiomegaly caused by various cardiovascular abnormalities tended to be higher than the normal values. Although there are some limitations of the methodology based on the half-space model, and fetal orientation may influence the magnitude of the dipole, making it smaller, fMCG recorded with a multichannel superconducting quantum interference device system is a clinically useful tool for noninvasive, prenatal, and electrical evaluation of fetal cardiac hypertrophy. (1) in 1974, the magnetic field generated by the fetal heart has been measured noninvasively with satisfactory waveforms. MCG requires no pasting of electrodes to the fetal body surface and is completely noninvasive to both fetus and mother. MCG signals from the fetal heart are considered to be minimally affected by the electrical conduction properties of the tissue around the heart (2, 3). In fact, time intervals can be obtained with satisfactory signal-to-noise ratio even after the development of vernix caseosa in the second half of gestation. A number of studies, including ours, defined the developmental changes and normal ranges of various time intervals on the fMCG in uncomplicated pregnancies (4 -6). However, the amplitude of the fMCG waveform has not been fully investigated (7), although it is another important variable used for the diagnosis of fetal heart diseases. One reason for this rare application is that the amplitude of fMCG measured on the maternal abdomen does not necessarily reflect the maximum value of myocardial current because of the effects of the depth and orientation of the heart. Furthermore, these biases are not easily corrected as the fetus may move during measurement.We attempted to approximate the magnitude of the onecurrent dipole of the fetal heart based on the maximum value of fMCG data obtained with a multichannel SQUID system and the depth of the fetal heart determined by echocardiography in normal pregnancies. We then used these control values to assess magnitude abnormalities in fetuses with cardiomegaly resulting from excessive volume loading in cardiac ventricles. Using bo...