Longevo Premium
Personalized medicine
It starts with your DNA
The same genetic content as Longevo, with medical consultation before and after the test and annual clinical reevaluation of data for four consecutive years.
Recent data shows a worrying rise in serious illnesses in younger adults
"Cases of cancer in young adults up to 50 years old increases 284% between 2013 and 2024."
"The prevalence of Stroke in young and middle-aged adults is on the rise significantly in the last decade."
"The heart attacks are becoming more common in younger people, especially women."
Maximum precision
Analysis based on whole genome sequencing to prevent +100 diseases.
Personalized journey
Pre-test medical consultation and post-test medical consultation to contextualize the results.
Four years of update
Annual clinical reassessment of data already generated for four consecutive years, without new annual sequencing.
Conventional check-ups look at the present
The Longevo Premium anticipate your future
Identify silent risks that do not appear in traditional check-ups, allowing for smarter decisions today.
More than a test, a long term plan for your health, anticipating decades of care.
Designed for those who have little time and high responsibility.
What the Longevo Premium analyze?
Genetics applied to anticipate risks, guide medical decisions and build a personalized plan for your health.
Mapping of genetic risks
Anticipation of predispositions related to cancer, cardiovascular, metabolic, neurodegenerative and inflammatory diseases.
Pharmacistgenetics
Identification of how your body responds to medications, helping doctors choose more effective and safe treatments.
health and longevity
Sleep, exercise response, stress, inflammation and healthy aging, with a focus on long-term quality of life.
It's not just a test
A medical journey personalized
Initial medical assessment
Through our concierge service, schedule your initial assessment online with specialist doctor to understand your history, lifestyle, health goals and family context.
Premium experience without commuting
sample collection at home, at the time fits your schedule, following strict laboratory quality standards.
Advanced genomic analysis
O same genetic content as Longevo, with sequencing performed once and specialized interpretation.
Return medical evaluation
You don't just receive a technical report. A specialist doctor interprets your results and builds, with you, a personalized long-term plan for your health online.
Premium Differential
Your data revisited for four years
After the return medical consultation, the genetic data already produced undergoes an annual clinical reevaluation for four consecutive years. This update does not mean a new sequencing nor does it include new annual consultations.
Who leads your Longevo Premium
Dr. João Bosco de Oliveira
Medical Director and Founder • Neogenomics
CRM 12563-PE • EQR 8733
A specialist doctor with more than 20 years of experience in genomics applied to clinical practice, Dr. João Bosco was the founder of Genomika Diagnósticos — acquired by Hospital Israelita Albert Einstein in 2017 — and Neogenomica, where he leads a team of geneticists, the medical strategy and the scientific curation of Longevo Premium.
He led the largest genomics project for rare diseases in the country, Genomas Raros, sequencing more than 10 thousand patients.
Its focus is to transform genetic data into clear decisions for prevention, diagnosis and therapeutic management, always with an ethical and patient-centered approach.
What do you get
The genetic content of Longevo in an expanded journey: pre-test medical consultation, post-test medical consultation and annual clinical reassessment of the same data for four consecutive years.
- Pre-test medical consultation and post-test medical consultation
- Whole genome sequencing
- Clear and contextualized clinical interpretation
- Annual clinical reassessment of data for four consecutive years
- Exclusive service via concierge
Hire the most advanced checkup of modern medicine
Take the next step towards healthcare based on personalization and prevention.
Proceed to purchase
Frequently asked questions
Hereditary Cancer Risk: Breast cancer, ovarian cancer, prostate cancer, bowel (colorectal) cancer, Lynch Syndrome, thyroid cancer, adrenal cancer, pancreatic cancer, skin cancer, melanoma, mesothelioma (pleural/peritoneal), choroidal melanoma (eye), systemic mastocytosis, skin hyperpigmentation, sarcomas, brain cancer, adrenocortical carcinoma, leukemias, endometrial cancer, kidney cancer, polyps gastrointestinal, pulmonary cysts, fibrofolliculomas, neurofibromas, malignant peripheral nerve sheath tumors, optic gliomas, vestibular schwannomas (bilateral), meningiomas, ependymomas, hereditary diffuse gastric cancer, pleuropneumoblastoma (PPB), multinodular goiter, retinoblastoma, osteosarcoma, aggressively evolving rhabdoid tumors in the central nervous system, astrocytomas subependymal giant cells (SEGA).
Heart Health: Heart muscle diseases (cardiomyopathies), heart failure, changes in heart rhythm (arrhythmias), sudden cardiac arrest, blood vessel diseases, aneurysm, Marfan Syndrome, metabolic diseases affecting the heart, Fabry disease (accumulation of fat), Pompe disease (accumulation of sugar), cardiac amyloidosis (accumulation of proteins).
Blood Health and Coagulation: Tendency to clots (thrombophilia), deep vein thrombosis, pulmonary embolism, tendency to bleed, hemophilia.
Metabolism: Hereditary high cholesterol, iron accumulation (hemochromatosis), Wilson's Disease (copper accumulation), cellular accumulation diseases, Pompe Disease (sugar accumulation in muscles), biotinidase deficiency (a vitamin that the body cannot recycle), MODY diabetes, urea cycle, alpha-1 antitrypsin deficiency.
Muscles, bones and development: Bones and connective tissue, muscular diseases (dystrophies), Duchenne muscular dystrophy, heart formation.
Nervous System: Neurodevelopment, neurofibromatosis, tuberous sclerosis, cognitive health and aging, Alzheimer's.
