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 …

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

CMA is recommended for individuals thought to have a medical condition associated with a chromosomal deletion or duplication. A missing or extra piece of chromosomal material can …

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

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 …

Your health care provider has ordered a genetic test called a microarray (MY-cro-a-ray) analysis. The test is also known as chromosomal microarray, whole genome microarray, array …

ng health, learning or development. WHAT IS CMA TESTING? Chromosome microarray (CMA) testing is a genetic test that can fi. d extra or missing pieces of chromosome material or DNA. …

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

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 …

Chromosomal microarray (CMA) is a high-resolution method for detecting copy number changes (gains or losses) across the entire genome in a single assay and is sometimes called a …