Understanding and diagnosing the potential causes of genetic conditions is an essential first step in optimizing an effective treatment plan. CMA is recommended for individuals thought to have a …

Follow-up testing for individuals with unexplained developmental delay or intellectual disability, autism spectrum disorders, or congenital anomalies with a previously normal conventional chromosome study.

This array is designed to identify numeric chromosomal abnormalities, unbalanced structural rearrangements, and copy number changes genome-wide in regions of known clinical significance …

Chromosomal microarray (CMA) is increasingly utilized for genetic testing of individuals with unexplained developmental delay/intellectual disability (DD/ID), autism spectrum disorders (ASD), or …

Miller DT, et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Chromosomal Microarray Analysis provides comprehensive genetic testing for the most common chromosomal conditions as well as a large number of severe genetic conditions not detected by …

A chromosomal microarray analysis, also called microarray or array, is a type of genetic test that looks for missing or extra portions of a chromosome. We call these “deletions” or “duplications.” In this …

Aug 5, 2025 · What is Chromosomal Microarray Analysis? Chromosomal microarray analysis (CMA) is a high-resolution genetic test. It detects very small missing or extra pieces of chromosomes, known as …

Dec 20, 2023 · Chromosomal microarray analysis, also known as CMA, is a powerful diagnostic technique used to detect and analyze changes in an individual’s chromosomes. It allows researchers …

IN SUMMARY Chromosome microarray (CMA) testing is a detailed genetic test that can look for extra or missing pieces of genetic material or DNA The test can be done on a blood, saliva or other tissue …