How can we help?
Six specialist care areas joining pediatric neurology, inherited metabolic disease and genetic diagnosis. Start from what you have noticed in your child, and we will point you to the closest area.
Assessment of movement and learning development, and of any change in skills your child already had.
Review of your child’s history and tests, and follow-up care for inherited metabolic conditions.
Understanding your child’s seizures, reviewing previous reports and following the right care plan.
A careful look at your daughter’s development, a clinical assessment and review of genetic reports.
Explaining genetic reports alongside your child’s examination, and talking through results and next steps.
Ongoing follow-up of your child’s needs, coordinating medical and therapy steps with your family.
One approach across every specialty
We start with your observations and your child’s development since birth.
A careful assessment of movement, communication and skills.
Only tests that change decisions: metabolic, genetic or imaging.
A written plan covering treatment, nutrition and rehabilitation.
Not sure which specialty?
Describe what you have noticed in your request, and the clinic team will guide you to the right next step.
