
pmid: 2038598
AbstractWe report two cases of prenatal detection of lissencephaly by high‐resolution ultrasound. The first case studied was referred for high‐risk obstetrical management and serial antenatal ultrasounds because of a family history of lissencephaly in an unresolved chromosomal abnormality. Diagnosis of a smooth gyral pattern consistent with lissencephaly was made at 32 weeks' gestation. The second case was referred for prenatal ultrasound because of a size versus dates discrepancy. The ultrasound examination showed a smooth gyral pattern at 31.5 weeks. In light of this ultrasound finding, a fetal blood sample was obtained and a chromosomal abnormality reported, confirming the diagnosis. To our knowledge, these cases represent the first report of the sonographic prenatal diagnosis of cerebral agyria or lissencephaly.
Adult, Chromosome Aberrations, Brain Diseases, Fetal Growth Retardation, Pregnancy Trimester, Third, Chromosome Disorders, Syndrome, Ultrasonography, Prenatal, Fetal Diseases, Pregnancy, Microcephaly, Tetralogy of Fallot, Humans, Female, Fetal Death, Chromosomes, Human, Pair 17
Adult, Chromosome Aberrations, Brain Diseases, Fetal Growth Retardation, Pregnancy Trimester, Third, Chromosome Disorders, Syndrome, Ultrasonography, Prenatal, Fetal Diseases, Pregnancy, Microcephaly, Tetralogy of Fallot, Humans, Female, Fetal Death, Chromosomes, Human, Pair 17
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