Pre-pregnancy screening for couples

  Name of services Additional (if necessary)

Initial consultation with a therapist
  • Analysis of family and personal history, vaccination history, patient complaints
  • Blood pressure measurement. BMI calculation. Drawing up an individual examination plan
Consultation with a geneticist, collection of family history, analysis of family medical history
Consultation of an otolaryngologist
Consultation with an ophthalmologist
Dentist visit
  • endocrinologist,
  • cardiologist,
  • allergist,
  • mammologist,
  • hematologist;
  • gastroenterologist;
  • surgeon;
  • orthopedist;
  • dermatologist
General blood test, general urine test, biochemical blood test (total protein, albumin, ALT, AST, direct/indirect bilirubin, glucose, glycated hemoglobin; creatinine, urea, TSH, T3, T4, TORCH complex);
Determination of blood group and Rh factor;
  • endocrinologist,
  • Hemostasiogram,
  • homocysteine,
  • cardiolipin antibodies,
  • lupus anticoagulant;
  • tension of immunity to vaccinated infections;
  • X-ray of the chest organs;
Ultrasound:
  • pelvis,
  • mammary glands,
  • thyroid gland;
  • abdominal cavity and kidneys;
  • echocardiography;
  • Duplex scanning of the veins of the lower extremities;
  • Transcranial Dopplerography of cerebral vessels;
  • Dopplerography of brachiocephalic vessels;
Obstetrician-gynecologist consultation, examination
  • examination of flora and presence of atypical cells
  • extended colposcopy
  • Ultrasound of the pelvic organs,
Consultation with a urologist
  • Spermogram
DNA diagnostics of common polymorphisms predisposing to thrombophilia
HIV, RW, hepatitis B and C, PCR for sexually transmitted infections
Molecular diagnostics of frequent polymorphisms in the genes of folate cycle enzymes (MTHFR, MTRR, MTR), predisposing to thrombophilia, chromosome nondisjunction in meiosis, congenital malformations of the nervous system, heart and urogenital tract
DNA diagnostics of common mutations in the genes of common hereditary diseases
Repeated consultation with a geneticist with an assessment of the risk of developing frequent multifactorial conditions in those consulting, taking into account personal and family history, calculation of the risk of hereditary diseases (in the case of a family history), an individual scheme for periconceptional prevention of congenital malformations in the fetus.
  • Study of the couple’s karyotype;
  • HLA typing;
  • DNA diagnostics of monogenic hereditary diseases
  Final consultation with a therapist, development of an individual preventive plan

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