Genetic Causes
Screens for inherited genetic and chromosomal variations linked to developmental conditions
Chromosomal Microarray (CMA 750K)
Detects chromosomal gains, losses, and structural variations at high resolution across 750,000 markers. A standard first-tier genetic test for developmental delay.
Whole Exome Sequencing
Sequences the protein-coding regions of the genome, roughly 20,000 genes, to identify genetic variants linked to developmental conditions.
Fragile X (FMR1)
Screens for the genetic mutation responsible for Fragile X syndrome, the most common inherited cause of intellectual disability and a known autism-associated condition.
MTHFR Polymorphisms
Checks for variations in the MTHFR gene, which affects how the body processes folate.

