Repronim2020-05-23T14:18:06+02:00

ReproNIM®

ReproNIM® is a study of carriers (or genetic compatibility test) that allows predicting a couple’s risk of transmitting certain diseases to their offspring. Using a combination of next generation massive sequencing (NGS, Next Generation Sequencing) and other molecular techniques, this test analyzes genes associated with recessive and X-linked diseases.

The selection of the studied diseases is made based on their clinical relevance, incidence and recommendations of the scientific societies.

With respect to these criteria and to be able to adapt to the different needs of specialists and patients, ReproNIM offers two types of analysis : ReproNIM® Focus and ReproNIM® Carrier.

ReproNIM® Carrier

Genetic compatibility test aimed at the study of more than 130 recessive or X-linked diseases:

  • Clinically relevant
  • Early onset
  • Selected following the recommendations of scientific societies

Who is it for?

When it is necessary to know the status of carriers of mutations in genes associated with genetic diseases in biological progenitors:

  • Egg cell donors
  • Egg cell recipients
  • Couples who wish to be parents
Delivery of results: 20 working days from receipt of the sample.
Reference:
REP1001

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ReproNIM® Focus LX

Genetic compatibility test aimed at the study of 16 recessive or X-linked diseases.

  • Clinically relevant
  • Early onset
  • With greater frequency of carriers in the healthy population
  • Selected following the recommendations of scientific societies

Who is it for?

  • Egg cell donors
  • Egg cell recipients
  • Couples who wish to be parents
Delivery of results: 20 working days from receipt of the sample.
Reference: REP1004

Contact us

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