, vol. 7, issue 11, 2011.
Background, congenital anomaly is a defect that is present at birth, and can result from either genetic, environmental factors, or both. Aim, was to explore the risk factors which may lead to fetal congenital anomalies. Design, a descriptive research design was adopted. Sample, a total of 100 pregnant women was recruited according to the following criteria: pregnant in a fetus with a congenital anomaly; at any reproductive age; no specific gravidity or parity; single or multiple gestations. Setting, Fetal Medicine Unit at El-Manial Maternity Hospital. Tools, two tools were constructed and filled in by the researchers: 1) Ultrasonographic fetal assessment record 2) structured interview schedule. Results, age range of the pregnant women were 17-44 years with a mean of 26.52 +5.48 years old. Twelve percent of them cannot read and write while, 22% had university education. Renal anomalies, central nervous system (CNS), muscloskeletal, cardiovascular, and gastrointestinal anomalies were the most common congenital anomalies constituted 38%, 31%, 20%, 10%, 8% respectively of the total anomalies. Regarding to risk factors for congenital anomalies, 44% of the pregnant women had first degree consanguinity, 17% had a family history of a congenital anomalies, 19% had a previous child with a congenital anomalies, 33% gave a history of consuming drugs during present pregnancy, 21% of the pregnant women live near industrial source and 22% of them experienced infection during present pregnancy. In conclusion, renal, CNS and muscloskeletal anomalies were the most common type of congenital anomalies. Positive consanguinity, family history for congenital anomalies, previous child with a congenital anomaly, consuming drugs during pregnancy, living near industrial source and exposure to infections during pregnancy, were the most common risk factors associated with congenital anomalies. Recommendations, premarital examination for consanguineous marriages should be encouraged. Antenatal care is very important for suspecting and early detection of congenital anomalies.