PRENATAL STUDIES

The possibility of knowing if everything is fine

PRENATAL STUDIES [PRENAT]

RULE OUT IF YOUR BABY CARRIES A CHROMOSOMAL ABNORMALITY

PRENAT-BLUE
logo prenatal en azul

For any woman

Screening for common aneuploidies:

  • Fetal sex and sexual aneuploidies
  • More common trisomies:
    • Down syndrome (T21)
    • Edwards syndrome(T18)
    • Patau syndrome (T13)
  • Only 5ml of blood
  • From the 10th week of gestation

Results en 4 - 7 days

ORDER
PRENAT-GOLD
logo prenatal en oro

For more curious women

Screening for all aneuploidies and CNVs:

  • Fetal sex and sexual aneuploidies
  • More common trisomies (T21, T18, T13)
  • Aneuploidiess in any chromosome
  • CNV detection:
    Micro-deletions/duplications
  • Only 5ml of blood
  • From the 10th week of gestation

Results in 4 - 7 days

ORDER

With the purchase of a prenatal study you will have 5% discount on any subsequent study.

WHAT IS A PRENATAL STUDY?

prenatal ecography

PRENAT is a Non-Invasive Prenatal test (NIPT) that, with just 5 ml of maternal blood, can detect if your fetus has any chromosomic abnormality.

This is made possible by the presence of cell free fetal DNA in the mother's blood, which is isolated and analysed through massive parallel sequencing (MPS) technology.

Sequencing of the fetal genome allows the identification with high sensitivity and specificity of the sex or sexual aneuploidies, the presence of common trisomies and other less common aneuploidies, and micro-deletions/duplications.

WHAT SYNDROMES AND ANOMALIES CAN BE DETECTED?

Fetal sex (XX o XY) or sex chromosome aneuploidies
⇨ X monosomy or Turner syndrome (karyotype 45X0), Klinefelter syndrome (karyotype 47XXY), Jakob syndrome (karyotype 47XYY).

More frequent aneuploidies
⇨ Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), Patau syndrome (trisomy 13).

Aneuploidies in the other autosomes (non sexual chromosomes)
⇨ Trisomies of chromosomes 7, 15, 16, 22, 3, 8, 9, 20, 10, 2, 14, 4, 11, 6, 5, 12.

Micro-deletions/duplications (CNVs) in any chromosome
⇨ Di George's, Van der Wouden's, Cri-du-chat's, Jacobsen's, Angelman's, or Prader–Willi's syndromes.

chromosomes, aneuloidies

WHEN TO DO IT AND WHO SHOULD DO IT?

pregnant woman

Any pregnant woman from the 10th gestational week, but most of all in the following cases:

  • Advanced maternal age
  • High risk result during the biochemical screening
  • Ultrasound findings suggestive of chromosomal abnormalities
  • Previous history of pregnancy with chromosomal abnormality
  • As front-line approach to assessing early pregnancy losses

TECHNICAL SPECIFICATIONS

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Screening of the entire genome

Detailed and highly sensitive fetal fraction quantification

Technical accreditation UNE-EN-ISO 15189 and equipment with CE-IVD marking

Less than 0.1% failure rate and false positive rate

Conducted in Spain, results in less than 1 week

In high-risk results, FREE confirmation by QF-PCR or CGH-array from an amniotic fluid sample

Suitable for any BMI, ethnic group, in vitro fertilization and egg donation

Study of possible gestational losses

Sensitivity 95% - 99.9%, Specificity 99.8% - 99.9%

Genetic counseling pre- and post-study

HOW DOES THE PROCESS WORK?

Very simple!

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1. Order the test through our website

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2. You get the consents by email and an appointment

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3. Blood collection at a medical center or at home

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4. We process the sample in the laboratory

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5. Delivery of results and genetic counseling