Cytogenetic Testing

Clinical Indicators fro Cytogenetic Testing (Chromosome Analysis)


Chromosome analysis is recommended as a routine method to diagnose (consider or rule out) genetic contributions in cases of different conditions:

  • Stillbirth and family history of neonatal deaths

  • Identification of the newborn’s sex in cases of abnormal genitalia

  • Growth- and development-related problems identified at an early age:

  • Growth and physical development delay;
  • Dysmorphic features;
  • Multiple malformations;
  • Short stature;
  • Underdeveloped or ambiguous genitalia;
  • Intellectual disability;
  • Delayed sexual development.
  • Infertility-related conditions:

  • Primary amenorrhea;
  • Secondary amenorrhea;
  • More than two self-inflicted abortions;
  • Abnormal spermatogenesis.

Family History – if a patient’s first-degree relative has a chromosome abnormality, the patient must complete chromosome analysis;

Advanced Maternal Age Pregnancy – (in women after 30-35) is a risk factor contributing to chromosome abnormalities, which is why prenatal screening and, if necessary, diagnostic of possible chromosome abnormalities of the fetus must be completed.



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Our Tbilisi office has moved!

Our official address is 23 Sulkhan Tsintsadze Street (former Saburtalo Street), though the map instructs to exit toward 9 Tsintsadze Street. After making a turn, you will see our road sign and 5-story building.

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To plan consultations with ReproART Fertility Specialist, please set an appointment in advance or request more information.

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