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Updated: Apr 28, 2026

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
Published on: February 21, 2015
Two cases of Scimitar syndrome associated with multiple congenital skeletal anomalies and lacking abnormalities by
Isaac E Lloyd1, Leslie R Rowe, Lance K Erickson
11 Department of Pathology, University of Utah, 15 North Medical Drive East, Suite #1100, Salt Lake City, UT 84112, USA.
Abstract:
Scimitar syndrome is a congenital anomaly occurring in approximately 1/50,000 births, consisting of partial anomalous pulmonary venous return, right lung hypoplasia, and several associated defects. The condition generally has significant morbidity and mortality, but the underlying cause is poorly understood. In this report, we describe 2 autopsy cases of Scimitar syndrome associated with multiple skeletal anomalies and attempt to characterize possible genetic abnormalities in this condition. In light of these findings, we discuss the embryology and direct timing during development of the anomalies associated with this syndrome.
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