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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News

REPROART CLINIC PAPER IN THE SCIENTIFIC JOURNAL “HUMAN REPRODUCTION”

14/04/2020 By magda

Despite the global situation caused by COVID-19, doctors and scientists continue their work. We would like to inform you that in one of the leading scientific journals in our field- "Human Reproduction", a scientific paper of fertility specialists and embryologists of our clinic has been published.

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