CNS 2020 presentation: Distinguishing pediatric movement disorders: Uncovering aromatic L-amino acid decarboxylase (AADC) deficiency
View our symposium presentation at
CNS 2020, which discusses making a differential diagnosis of AADC deficiency Understand how the symptoms of cerebral palsy, epilepsy, movement disorders and other pediatric neurotransmitter disorders may clinically resemble AADC deficiency, complicating diagnosis Real-world clinical experiences of diagnosing AADC deficiency are discussed Review the current management strategies and emerging therapies, including data for an investigational gene therapy, for the treatment of AADC deficiency
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GL-AADC-0648 | March 2021
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