I. Nulman et al., FINDINGS IN CHILDREN EXPOSED IN-UTERO TO PHENYTOIN AND CARBAMAZEPINE MONOTHERAPY - INDEPENDENT EFFECTS OF EPILEPSY AND MEDICATIONS, American journal of medical genetics, 68(1), 1997, pp. 18-24
Our objective was to evaluate the patterns of malformations in childre
n exposed in utero to phenytoin (DPH) and carbamazepine (CBZ) monother
apy, and to compare them prospectively with matched mother-child pairs
exposed to nonteratogens, and to separate the effects of antiepilepti
c drugs (AEDs) from those of epilepsy by collecting groups of untreate
d epileptics and those treated with DPH and CBZ for conditions other t
han epilepsy, This was a prospective, controlled, and blinded observat
ional study. Thirty-six mother-child pairs exposed to CBZ monotherapy,
34 pairs exposed to DPH monotherapy, and 9 nonmedicated epileptic wom
en and their children were compared with matched mother-child pairs ex
posed to nonteratogens, The control mothers were matched for maternal
age, time of consultation, obstetric history, and socioeconomic status
(SES), One main outcome measures a ''blinded'' morphological assessme
nt of the offspring. We found that minor anomalies were significantly
more common among children of epileptics on either drug (P = 0.01) and
among DPH-treated nonepileptic offspring (P = 0.03), Among epileptics
, the relative risk for minor anomalies following DPH (2.1) was simila
r to that after exposure to either DPH (P = 0.006) or CBZ (P = 0.01).
Increased rates of hypertelorism were detected among DPH-exposed offsp
ring, High forehead, frontal bossing, malar hypoplasia, epicanthus and
micrognathia were associated with untreated epilepsy, as well as with
DPH and CBZ treatment. (C) 1997 Wiley-Liss, Inc.