Cornelia de Lange syndrome is characterized by distinctive craniofacial features, developmental delays, variable congenital malformations, and growth retardation. Several conditions have considerable overlap with CdLS, including Coffin-Siris syndrome, Rubinstein Taybi syndrome, Robinow syndrome, and Roberts syndrome. The Cornelia de Lange PLUS Sequencing Panel offers sequencing of 21 genes associated with CdLS and related disorders.
Our Cornelia de Lange Syndrome PLUS Sequencing panel includes sequencing of 21 genes (see information sheet for more details).
Any gene in the Cornelia de Lange Syndrome PLUS Sequencing panel can also be ordered separately. Please contact us directly for cost and CPT code information.