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Karyotype (Chromosome)

Karyotype (Chromosome)

A cytogenetic test examining the number and structure of chromosomes to detect abnormalities related to fertility, development, or genetic disorders. Identifies chromosomal changes such as deletions, duplications, or translocations that can influence reproductive health or congenital conditions.

  • Sample type: Venous blood (home draw supported).
  • Fasting: Not required.
  • Turnaround time: 2–4 weeks.
  • Who it’s for: Individuals undergoing fertility evaluation, pregnancy planning, or genetic condition screening.
AED 2,493.75

This test evaluates:

  1. Chromosome number abnormalities (extra or missing)
  2. Structural rearrangements (translocations, inversions, deletions, duplications)
  3. Sex chromosome variations
  4. Large-scale genetic changes impacting development or fertility
  1. Full chromosomal analysis (46 chromosomes)

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