NON INVASIVE PRENATAL DIAGNOSIS

|NON INVASIVE PRENATAL DIAGNOSIS
NON INVASIVE PRENATAL DIAGNOSIS 2018-06-27T11:38:49+00:00

Project Description

It diagnoses early and in a non-invasive way Down´s syndrome and other chromosomal alterations in the fetus

With this test we reduce the risk of unnecessary invasive and potentially dangerous procedures.

It is performed using a blood test from the tenth week of gestation; at which state the placenta is fixed to the uterus and cells pass from there into the mother’s blood. We will study the chromosomes and fetal DNA from these cells.

Prior to the procedure, we perform an ultrasound scan to assess gestational age and confirm fetal vitality

  • It detects trisomies 21, 18, 13 and alterations in the sex chromosomes. We also have more advanced tests that diagnose those conditions and also other less frequent diseases.

  • Trisomy 21 (Down syndrome) is the most frequent. It occurs in 1 out of every 700 pregnancies and increases especially with maternal age.
  • The results have a diagnostic capacity higher than 99% for Down syndrome and 95% for trisomies 13 and 18.
  • The false positive rate is less than 0.1%. Being over 0%, after a positive result, we must confirm the diagnosis with an invasive genetic study (amniocentesis or chorionic villus).

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MULTIDISCIPLINARY TEAM

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PROFESSIONAL AND HUMAN TREATMENT

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Monday – Friday 10:00 – 21:00

Saturday 10:00 – 14:00

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