Children experiencing a complex mix of symptoms including seizures and developmental delays may have an underlying genetic condition. Knowing which genes may be contributing to the symptoms can inform precision medicine and other benefits.
Download our whitepaper to find out who may be missing a genetic diagnosis.
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Disclaimer
Please note that AmbitCare provides this information for the benefit of the rare disease community. AmbitCare is not a medical provider nor a health care facility. AmbitCare can neither diagnose any disease or disorder nor endorse or recommend any specific medical treatments. Individuals must rely on the personal and individualized medical advice of their qualified health care professionals before seeking any information related to their particular diagnosis, cure, or treatment of a condition or disorder.