Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature

摘要

Trisomy of the short arm of chromosome 17 is a rare genomic disorder. The clinical features of complete trisomy 17p syndrome have been described. Most cases of this syndrome have been found in infants and children, but only a few cases were found by ultrasound in the prenatal period.