Sistemas Genómicos

Sistemas Genómicos Empresa a la vanguardia de la biotecnología.

31 AUG | World Day of Obstetrics and PregnancyOn this day, we acknowledge the work of obstetricians, midwives and multid...
31/08/2025

31 AUG | World Day of Obstetrics and Pregnancy

On this day, we acknowledge the work of obstetricians, midwives and multidisciplinary teams who care for the mother–baby bond. At Eurofins we drive progress in prenatal diagnostics, fetal medicine and reproductive genetics — supporting pregnancies with greater precision and safety. Because every beginning matters.

28 AUG |  World Turner Syndrome DayOn World Turner Syndrome Day, Eurofins reaffirms its commitment to increasing awarene...
28/08/2025

28 AUG | World Turner Syndrome Day

On World Turner Syndrome Day, Eurofins reaffirms its commitment to increasing awareness of this genetic condition. Through early diagnosis, genetic research and clinical support, we aim to improve the quality of life of girls and women affected by this rare chromosomal disorder.

Very sample represents a life. At Eurofins we believe diagnostics go beyond technology — they are deeply human. We suppo...
19/08/2025

Very sample represents a life. At Eurofins we believe diagnostics go beyond technology — they are deeply human. We support healthcare professionals and institutions with specialised services and fast clinical insight.

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11 AUG | | World Nutritionist DayAt Eurofins we value the essential role of nutritionists in preventive medicine, chroni...
11/08/2025

11 AUG | | World Nutritionist Day

At Eurofins we value the essential role of nutritionists in preventive medicine, chronic disease management and personalised patient care. We join in recognising these professionals who, through the science of nutrition, promote health, balance and quality of life.

22 Jul | World Brain DayAt Eurofins we join the global recognition of World Brain Day by highlighting the critical role ...
22/07/2025

22 Jul | World Brain Day
At Eurofins we join the global recognition of World Brain Day by highlighting the critical role of prevention, early diagnosis, and research in brain health.

As strategic partners in the healthcare sector, we reaffirm our commitment to developing advanced diagnostic solutions that contribute to a deeper understanding, detection, and management of complex neurological disorders.

We collaborate with clinicians, hospitals, and research centres to drive more precise and personalised medicine in the neurological field.

Because a healthy brain is key to a fulfilling life.
Knowledge, innovation, and collaboration at the service of brain health.



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We continue to be your partner in clinical diagnostics, genetics, and pathology. Now as Eurofins Spain. Join us at Eurof...
15/07/2025

We continue to be your partner in clinical diagnostics, genetics, and pathology. Now as Eurofins Spain. Join us at Eurofins Megalab

Genetics, genomics, pharmacogenetics. We continue to provide expert services from Eurofins Megalab👉 Follow us at Eurofin...
08/07/2025

Genetics, genomics, pharmacogenetics. We continue to provide expert services from Eurofins Megalab

👉 Follow us at Eurofins Megalab to stay connected.

New challenges, same principles: scientific rigour, evidence and commitment. Eurofins Spain strengthens clinical researc...
04/07/2025

New challenges, same principles: scientific rigour, evidence and commitment. Eurofins Spain strengthens clinical research and advanced diagnostics.

👉 Follow us at Eurofins Megalab

Rare diseases affect a small part of the population, with a prevalence of less than 5 per 10,000 inhabitants. In the Eur...
28/02/2025

Rare diseases affect a small part of the population, with a prevalence of less than 5 per 10,000 inhabitants. In the European Union, 27 and 36 million people live with one of the 6,000 to 8,000 known rare diseases. Some affect only a few patients; others may affect up to 245,000 people. Approximately 80% of these diseases are genetic in origin, and 70% start in childhood, which underlines the importance of early and accurate diagnosis.

These conditions can be the result of inherited genetic mutations or spontaneous mutations and can range from monogenic diseases (caused by alterations in a single gene) to more complex diseases involving multiple genes and environmental factors.

On this World Rare Disease Day, we reaffirm our commitment to genetic and molecular research to advance our understanding of these conditions, leading to improved early diagnosis and more personalised care for patients and their families.

Asperger Syndrome, part of the autistic spectrum, is a disorder that involves the interaction between genetics, biology ...
18/02/2025

Asperger Syndrome, part of the autistic spectrum, is a disorder that involves the interaction between genetics, biology and environment. Its prevalence is higher in males, with four cases for every female, and it is estimated to affect between 1 and 5 people per 1,000 births. Moreover, its impact affects the individual, family, and social environment.

In the last 40 years, the prevalence of autism spectrum disorders (ASD) has increased, with 1 case per 100 births today, which in Spain represents more than 450,000 people. However, if we consider its effect on families, the figure exceeds 1 million.

Research has identified at least 200 genes associated with ASD, although this number could be as high as 2,000 due to the complexity of genetic interactions, which are also influenced by biological and environmental factors.

On this World Asperger Syndrome Day, we reaffirm our commitment to genetic research and the development of diagnostic tools that improve the lives of people with Asperger Syndrome and their families.

Childhood cancer represents a global health challenge, affecting thousands of children and adolescents every year. It is...
15/02/2025

Childhood cancer represents a global health challenge, affecting thousands of children and adolescents every year. It is estimated that around 400,000 children and adolescents aged 0-19 years suffer from cancer annually, highlighting the need to strengthen prevention and research.

Genetics plays a key role in childhood cancer, as some types of the disease have a hereditary component, where genetic mutations passed down in certain families can increase the risk. Understanding these genetic bases is key to identifying at-risk children and providing more accurate and personalised care. In addition, genetic testing and counselling are valuable tools for families with a history of childhood cancer, enabling them to assess risk, make informed decisions and plan effective prevention strategies.

On International Childhood Cancer Day, we reinforce our commitment to early detection, research and support for families. Prevention, access to advanced testing and personalised care are essential steps towards a more hopeful future for the little warriors facing this disease.

Congenital heart disease encompasses various abnormalities in the structure of the heart that are present from birth. Th...
13/02/2025

Congenital heart disease encompasses various abnormalities in the structure of the heart that are present from birth. These conditions represent one of the most common congenital disorders, with a significant prevalence also in the adult population.

According to epidemiological studies, 3 out of every 1,000 adults, which translates into approximately 120,000 adults in Spain, live with congenital heart disease.

What role does genetics play?
Genetics is a fundamental factor in the development of congenital cardiopathy:
- Inherited or spontaneous mutations: Some cardiac anomalies are due to genetic defects transmitted from parents, while others occur spontaneously during foetal development.
- Genetic and environmental interaction: Genetic and environmental factors often contribute to developing these conditions.

On World Congenital Heart Disease Day, we reinforce our commitment to research, prevention and early detection of these conditions.

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Ronda Guillermo Marconi, 6 Parque Tecnológico
Valencia
46980

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Nuestra misión

Contribuir a mejorar la calidad de vida de las personas con enfermedades hereditarias así como velar por la salud de las personas en materia de calidad alimentaria.