A karyotype test may be used to: Check an unborn baby for genetic disorders. Diagnose a genetic disease in a baby or young child. Find out if a chromosomal defect is preventing a woman from getting pregnant or is causing miscarriages.

What is karyotyping What are its uses?

Karyotyping is a test to examine chromosomes in a sample of cells. This test can help identify genetic problems as the cause of a disorder or disease.

What does karyotype test show?

Karyotype is a test to identify and evaluate the size, shape, and number of chromosomes in a sample of body cells. Extra or missing chromosomes, or abnormal positions of chromosome pieces, can cause problems with a person's growth, development, and body functions.