The pediatric neurogenetics program at Children’s Minnesota is a collaboration between kid experts from our neuroscience and genomic medicine programs, working in partnership with specialists at Noran Neurology and Minnesota Epilepsy Group.
Together we aim to understand how genetics contribute to various pediatric neurological and neurodevelopmental conditions as the underlying cause – and then develop personalized treatment plans that tailor therapeutic strategies to each child’s unique needs.
A comprehensive assessment of a child’s genetic diagnosis can be critical for making informed decisions about many neurological conditions, as well as possibly testing other at-risk family members to manage their care. Many families find genetic testing also to be empowering and helpful for understanding, treating and or managing a health condition that is common to multiple family members.
We offer easy scheduling for your child’s neuroscience needs.
We’re the only neurogenetics team in Minnesota that’s exclusively focused on kids, so even though this genetics stuff sounds complicated and maybe a little scary, we promise: we take really good care of kids (and other family members). Our multidisciplinary team approach makes sure you always have someone to answer your questions and provide the care you need. Contact us today for an appointment.
All genetic conditions are caused by changes in the body’s instructions, or genes. While genes are passed from parent to child, genetic conditions are not always inherited. Sometimes a new gene changes (mutates) in a child. Neurogenetic conditions are caused by gene changes that affect brain and nerve development and function. There are hundreds of neurogenetic conditions; some of the most common include epilepsy, hydrocephalus, brain malformations, and neurodevelopmental disorders.
Reach us 24/7 for patient referrals, consults, admissions and neonatal transport.
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