Karyotype analysis refers to the pairing and grouping of chromosomes to reveal whether the organism accords with the inherent chromosomal characteristics, so as to determine if the organism has chromosomal abnormalities. Our company provides a wide range of karyotype analysis methods and in-depth solutions to help you quickly grasp genetic information related to rare diseases.

Karyotype Analysis in Rare Disease

Karyotype reflects the chromosomal status of an individual. Karyotype analysis can detect whether there are abnormalities in chromatin length, centromere position, the ratio of long and short arms, and the presence or absence of satellites. Many rare diseases have obvious manifestations of chromosomal structural abnormalities, making it a strategy to determine the cause of diseases from a macroscopic perspective of genetics.

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