We are a Genomics-as-a-Service company, applying our end-to-end solutions to hand #genetic reports at the #clinical desk. We make #genomics accessible!
We are very happy to announce that CBR Genomics was elected to the TOP 10 EMERGING NEXT-GENERATION SEQUENCING COMPANIES IN EUROPE 🎊 🏆🎊
https://t.co/01kHGfgDCc
Fabry Disease is a multisystemic pathology, which means that it can affect several systems of our body 🧑⚕️
Essentially, Fabry Disease manifests in the cardiovascular ❤️ neurological 🧠 renal, and gastrointestinal systems 🤕
#fabry#fabridisease#april#cbrgenomics
Rare diseases are not that rare after all 🎗️
About 70% of rare diseases have a genetic origin 🧬 With pan adequate genetic analysis, these diseases can be screened before the appearance of the firsts symptoms.
This is what we aim for with our DNA.files BABY service – prevent
Statistical data indicates that Fabry Disease affects 1 in 40,000 to 117,000 male births. However, as with almost all rare diseases, the diagnostic capacity is low and the number of real cases is far from the statistics.
#fabry#fabrydiseade#april#awarenessmonth#dna#trends
Fabry disease is a rare and hereditary disease. It is caused by a mutation on the X chromosome and therefore it has a higher effect on males (XY) because they have only one X.
April is "Fabry Disease Awareness Month" and, as such, we launched a new section on this pathology. Throughout the month we will present Fabry Disease and demystify its condition. Ready to join? 😉
#fabry#fabrydiseade#april#awarenessmonth#dna#trends#life#future
The Human Genome has been fully mapped. The research was recently published by Science.
The final code counts with 3 billion letters, an absolutely huge number. If it took us 1 second to type each letter in the human genome, it would take us about 95 years to complete the task 🤯
With our DNA.files BABY service, it is possible to detect mutations in more than 500 genes, responsible for about 300 pediatric diseases of genetic origin 🧬
All of this, before the appearance of the first symptoms 👶
#baby#pregnant#pregnancy#cbr#dna#heritage#health
At the @WebSummit, we have a Community Room - "The Code of Life" - dedicated to information sessions on #Genetics and the (Future) Present of Personalised #medicine.
👉Join us today at 3:00 pm and 6:40 pm to participate and interact with our experts.
https://t.co/dNVopwuidO