Methimazole embryopathy: delineation of the phenotype
- PMID: 10076883
Methimazole embryopathy: delineation of the phenotype
Abstract
We report on a further case of congenital anomalies in a child exposed to methimazole during the first trimester of pregnancy (from first to seventh gestational week), and define a specific malformation pattern related to prenatal methimazole exposure and consisting of choanal and esophageal atresia, scalp defects, minor facial anomalies and psychomotor delay.
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