Array-CGH (microarray)

Chromosomal microarray detecting copy-number variants beyond karyotype resolution.

Copy-number variants with clinical interpretation.

Evidence: Well-established; prenatal exome maturing

cfDNA/NIPT is a highly accurate screening test for the common trisomies. Microarray and QF-PCR are first-line diagnostics on invasive samples, with prenatal exome adding yield in selected cases.

Limitations

cfDNA/NIPT is a screening test, not a diagnosis: a high-risk result requires confirmatory invasive testing, and performance for microdeletions is more limited than for the common trisomies.

Prenatal: published evidence

This test needs genetic counselling and written consent; your clinic confirms both at ordering.

• NIPT (cell-free DNA prenatal screening)

  Screens for trisomy 21, 18 and 13 from a maternal blood draw.

• Fetal Karyotype

  Full chromosome analysis of the baby.

• QF-PCR

  Rapid check for the most common chromosome conditions.

• Whole-Exome Sequencing

  Deep gene sequencing to find a suspected genetic cause.