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KMID : 0361719920030010088
Korean Journal of perinatology
1992 Volume.3 No. 1 p.88 ~ p.94
A Case of Prenatal Ultrosangraphic Diagnosis of Roberts Syndrome
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Abstract
Roberts syndrome is a rare autosomal recessive hereditary syndrome, characterized by profound pre-and postnatal growth reductions, symmetrical limb reductions of varying severity, and craniofacial abnormalities with infrequent survival beyond
infancy.
We report a case of Roberts syndrome diagnosed by antenatal ultrasonography with a brief review of literatures.
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