Opening Doors to Diagnosis: Chromosomal Microarray
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We are pleased to announce new reduced pricing for our Chromosomal Microarray (CMA). CMA is often used as a first-tier test for clinical diagnosis of patients with idiopathic intellectual disability, developmental delay, autism spectrum disorders and/or multiple congenital anomalies (Miller, D.T. et al. 2010).
Chromosomal Microarray, Test Code 2000, $990
Rapid Prenatal Chromosomal Microarray, Test Code 3780, $1390
Our chromosomal microarray test, CMA-ISCA, combines a total of 180,000 CGH and SNP probes to detect microdeletion and microduplication syndromes as well as regions with absence of heterozygosity (AOH) and uniparental disomy (UPD). The inclusion of SNP probes along with CNV probes improves the diagnostic yield of a CMA test.
We understand your patients are small and their blood is precious. By offering the most comprehensive sequencing menu in the U.S., additional molecular testing work-up can be ordered conveniently through one facility using the original patient specimen. Our reports are complete including lists of strong candidate genes for recessive disease within AOH regions.
We are committed to providing comprehensive, high quality, and affordable testing. We strive to provide the majority of tests results within 18 calendar days to aid in quicker clinical diagnosis. For rapid prenatal CMA, the great majority of tests are completed within 3 to 6 days
At PreventionGenetics, we have all your testing needs under one roof. Open doors to your patient's diagnosis starting with our chromosomal microarray. Put us to the Test!