12 studies
in just one test
We implement
NGS technology
In-house team
of medical geneticists
Pioneers in whole
genome sequencing
What do we do?
Our Excellence in Genetic Counselling and Personalised Medicine Service is aimed at improving your health on an ongoing basis.
Laboratorios Larrasa is a pioneer in Southern Europe with the most advanced technologies in Whole Genome Sequencing.
Thanks to DNA Sequencing, Bioinformatics Analysis, and the Knowledge and Experience of our entire team, we obtain the most accurate and complete biological information, so you can make informed decisions.
Why is it important?
Between 15-20% of the population has pathogenic variants associated with disease risk
About 5% of patients are hospitalised for adverse drug reactions
Approx. 20% of sudden cardiac deaths are caused by genetic abnormalities
About 20% of cancer cases are due to genetics and are related to hereditary factors
Between 15-20% of the population has pathogenic variants associated with disease risk
About 5% of patients are hospitalised for adverse drug reactions
Approx. 20% of sudden cardiac deaths are caused by genetic abnormalities.
About 20% of cancer cases are due to genetics and are related to hereditary factors
What are the health benefits?
¿Qué beneficios tiene para mi salud?
- Diagnósticos más precisos
- Reducción de reacciones adversas a medicamentos y ajuste de dosis.
- Instauración de tratamientos más precisos, eficaces y de forma más rápida.
- Prevención y detección temprana de enfermedades.
More accurate diagnoses.
Reduces adverse drug reactions and dose adjustment.
More precise, effective and faster treatments.
Prevention and early detection of diseases.
¿Qué beneficios tiene para mi salud?
More accurate diagnoses.
Reduces adverse drug reactions and dose adjustment.
More precise, effective and faster treatments.
Prevention and early detection of diseases
¿Qué beneficios tiene para mi salud?
More accurate diagnoses
Reduces adverse drug reactions and dose adjustment
More precise, effective and faster treatments
Prevention and early detection of diseases
How does the process work?
1.Simply give us a call and we will arrange an appointment for you with one of our Genetic Counselling specialists.
2.The doctor will take a saliva sample and send it to us together with the application form, the informed consent form and your medical history.
3.Your sample will then be processed in our laboratory, following the highest quality standards and in the shortest possible time.
4.Once we complete your genetic report, we will give it to the specialised doctor, who will provide you with individualised advice to help improve your health.
5.You will receive your Complete Genome Sequence, allowing you to be in control of your genetic information and to make informed decisions.
Simply give us a call and we will arrange an appointment for you with one of our Genetic Counselling specialists.
The doctor will take a saliva sample and send it to us together with the application form, the informed consent form and your medical history.
Your sample will then be processed in our laboratory, following the highest quality standards and in the shortest possible time.
Once we complete your genetic report, we will give it to the specialised doctor, who will provide you with individualised advice to help improve your health.
You will receive your Complete Genome Sequence, allowing you to be in control of your genetic information and to make informed decisions.
Impulsando vidas
Queremos ayudarte a tomar mejores decisiones.
Lucas, 36 (Francia)
“Con el estudio de mi genoma descubrí que tengo una variante genética que aumenta mi riesgo de trombosis, como viajo mucho en avión ahora trato de levantarme y moverme, me parece una información importante y que me permite prevenir fácilmente”
Olga, 48 (Reino Unido)
“Me sorprendió saber que tengo una variante que causa una enfermedad llamada hemocromatosis, por la cual el hierro se acumula en hígado, al principio me asusté, pero el médico me explicó que es posible tratarla y prevenir complicaciones. Estoy muy satisfecha porque gracias al estudio del mi genoma puedo prevenir una enfermedad que no sabía que podía tener”
Juan Pablo, 38 (Colombia)
“Después de un episodio de arritmia en altitud, mi cardiólogo me recomendó realizar una prueba genética que reveló una mutación relacionada con arritmia y fibrilación auricular. Desde entonces, he hecho check ups regulares y he adaptdo mi actividad física a esta nueva situación.”
FAQ
Thanks to this personalised medicine service, you will be able to:
– Predict and prevent hereditary diseases.
– Adapt treatments and medicines.
– Improve family planning.
– Optimise well-being and lifestyle.
The process takes about eight weeks from the time the sample is obtained in our laboratory until the molecular report is issued.
Our genome derivation test can be carried out at any age. From babies to adults, genetic information is priceless when it comes to protecting our health.
Our analysis is able to provide information on 12 studies using a single sample.
We offer interdisciplinary information on hereditary diseases, drug sensitivities, conditions that can be passed on to children, issues related to diet, sport, longevity, nutrition… and much more!
In addition, we also carry out customised studies for those patients who require them.
Our personalised medicine service is recommended for everyone. However, we would like to highlight a number of specific cases:
– When there is a family history of hereditary or genetic diseases.
– Patients with chronic diseases.
– Couples with fertility problems.
– Patients with illnesses with no known cause or with rare diseases.