Underlying karyotype abnormalities in IVF/ICSI patients

Reprod Biomed Online. 2008 Apr;16(4):514-22. doi: 10.1016/s1472-6483(10)60458-0.

Abstract

Cytogenetic investigations are performed in couples asking for IVF or intracytoplasmic sperm injection (ICSI) treatment. These serve a diagnostic purpose because male or female infertility might have a chromosomal origin. Chromosomal aberrations found in these patients include numerical abnormalities, such as Klinefelter syndrome, XYY karyotype or Turner syndrome and its variants; sex reversions, such as XX males or XY females; and also structural abnormalities, such as Robertsonian or reciprocal translocations and inversions. Finding the chromosomal origin of infertility in a patient also has a prognostic value because it aids the management of pregnancies obtained after IVF or ICSI and may lead to a proposal of prenatal or preimplantation genetic diagnosis.

Publication types

  • Review

MeSH terms

  • Chromosome Aberrations*
  • Disorders of Sex Development
  • Female
  • Fertilization in Vitro* / methods
  • Heterochromatin / genetics
  • Humans
  • Infertility / etiology
  • Infertility / genetics*
  • Infertility / therapy
  • Male
  • Polymorphism, Genetic
  • Pregnancy
  • Sex Chromosome Disorders / complications
  • Sex Chromosomes / chemistry
  • Sperm Injections, Intracytoplasmic* / methods

Substances

  • Heterochromatin