FirstSteps offers preventive genetic information that helps families and healthcare professionals understand potential genetic factors early, so they can support the child with knowledge, care and confidence.
5%
of children worldwide are born with a rare disease, most of which are genetic in origin
8,000
known genetic diseases, many of which are extremely rare
30%
of admissions to children's hospitals are associated with an underlying genetic condition
800
genetic diseases are now considered treatable, and this number continues to grow
5%
of children worldwide are born with a rare disease, most of which are genetic in origin
8,000
known genetic diseases, many of which are extremely rare
30%
of admissions to children's hospitals are associated with an underlying genetic condition
800
genetic diseases are now considered treatable, and this number continues to grow
About FirstSteps
Using advanced genetic analysis, we offer insights that can help identify potential health risks, developmental considerations, or inherited conditions early on. Our goal is not to replace medical care, but to support families and healthcare professionals with meaningful information that enables timely monitoring, prevention, and personalized care.
For a more certain future
Every family wants to give their child the best possible start.
First Steps helps by offering clarity—helping parents understand potential genetic factors that may influence their child's health and development. With this knowledge, families can:
Feel more confident about their child's future
Collaborate more effectively with healthcare professionals
Avoid unnecessary delays in evaluation or intervention
Focus on prevention, not just treatment
How it works
Three steps on how our genetic analysis and genome screening works
- 1
Consultation & Guidance
The process begins with clear and understandable information. Families receive an explanation of what FirstSteps is, what it examines, and what kind of information it can provide. All questions are addressed before any step is taken. Participation is entirely voluntary and proceeds only after informed consent is given.
- 2
Genetic Analysis
A small blood sample is collected using the heel stick test, a method commonly used in newborn screening worldwide. The procedure involves a gentle prick on the baby's heel to collect a few drops of blood. It is quick, safe, and performed by trained professionals, following established medical and safety standards. Any brief discomfort is minimal and temporary.
- 3
Results & Next Steps
The sample is analyzed using validated genetic analysis methods. Results are carefully reviewed and prepared in a clear, structured format, focusing on meaningful information rather than complex technical details. The aim is understanding—not overwhelming families with data.
We are here to support you
If you have questions or would like to learn more about how FirstSteps works, our team would be happy to talk with you.
Contact us