PREVENTIVE & DIAGNOSTIC STUDIES

THE POWER OF YOUR DNA IN YOUR HANDS

WORRIED ABOUT YOUR FUTURE CHILDREN'S HEALTH?

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PRENATAL GENETIC COMPATIBILITY STUDIES

1 in 300 children born to healthy parents develops one of the 3,200 known autosomal recessive genetic disorders, such as spinal muscular atrophy, Duchenne's muscular dystrophy or the Fragile-X syndrome.

Know your risk now and prevent that your future children inherit one of these 3,200 conditions with our PRECON studies, the most comprehensive carrier test on the market!

DIFFICULTIES TO HAVE CHILDREN?

INFERTILITY STUDIES

About 15% of couples in Spain suffer from infertility equally affecting men and women. Find out if your difficulties have a genetic explanation:

- Genetic sterility (fertilization issues)
- Inmunological incompatibility KIR/HLA (implantation issues)
- Genetic incompatibility (post-fertilization problems)
- Karyotype studies (chromosomal abnormalities)

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WISH TO RULE OUT CHROMOSOMAL ABNORMALITIES?

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Did you know that 1 in 700-800 newborns in Europe is born with Down syndrome? This risk significantly increases with maternal age.

Our non-invasive prenatal studies [PRENAT] accurately detect trisomies, other aneuploidies and micro-deletions as early as the 10th week of gestation. Includes Down's (T21), Edwards' (T18), or Patau's (T13) syndromes, Turner syndrome (X0), or Di George's, Angelman's, and Prader-Willi's syndromes, among others.

DOES YOUR CHILD HAVE AN UNDIAGNOSED CONDITION?

DIAGNOSIS OF PEDIATRIC DISEASES

1 in 100 babies are born with one of the more than 5,500 known rare genetic conditons, such as cystic fibrosis, neurofibromatosis or Huntington's disease.

A FAMILY-TRIO study is the most powerful tool to confirm if there is a genetic cause. This knowledge would allow the use of targeted and more effective treatments to improve your child's life.

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DO YOU SUSPECT HAVING A GENETIC CONDITION?

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EARLY DIAGNOSIS & PREVENTION

About 3 million people in Spain alone live with a genetic condition such as familial hypercholesterolemia, neurofibromatosis, cystic fibrosis, dilated cardiomyopathy, Marfan's or Noonan's syndrome, or thalassemias.

With PREVENT discover in a few weeks if your symptoms have a genetic origin, so you can apply more specific and targeted solutions.
You could also find out your genetic predisposition to cancer, Alzheimer's, Parkinson's or other degenerative conditions.

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HOW DOES IT WORK?

ALL FROM THE COMFORT OF YOUR HOME

muestras de saliva desde casa
NON INVASIVE

Collect your own saliva at home

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100% ONLINE

Save purchase from our platform

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HOME DELIVERY

We send you and pick up the collection kits

informe genetico con resultados
RAPID RESULTS

Reports ready in only a few weeks

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CONSULTATIONS

Counselling before and after study

WHY DO PEOPLE CHOOSE US?

For achieving our purpose of making families healthier and happier

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Passion about genetics

And its power to prevent diseases and improve patient's treatments

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Close & committed

We work with the heart to feel that we are part of your family plan

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Our reporting & counselling

Of the highest quality and scientific rigor. Always at your disposal

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Innovation & knowledge

We combine our knowledge with the latest technology

COMMITTED TO SCIENTIFIC RESEARCH

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Curious by nature
Active in research projects

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Special interest in improving calculations of the prevalence of carriers in the European population

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With your anonymized genetic data we collaborate with scientific progress

WE COLLABORATE WITH

accesible spain travel (AST)
AEPEF
Asociación X-frágil Madrid
Coalas
Duchenne Parent Project Spain
Clínicas Segura
creando una vida
Clínica Gineceo Murcia
Telegenomics

ARE YOU UNDECIDED, HAVE DOUBTS OR WANT TO KNOW MORE?

WE'RE HERE TO HELP!

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Tell us how to reach you here

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A geneticist will call you

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We will solve all your questions!