Severe Acute Motor Exacerbations (SAME) across Metabolic, Developmental and Genetic Disorders

Author:

Couto Blas12ORCID,Galosi Serena3ORCID,Steel Dora45,Kurian Manju A.45ORCID,Friedman Jennifer67,Gorodetsky Carolina89ORCID,Lang Anthony E.11011ORCID

Affiliation:

1. Edmond J. Safra Program in Parkinson's Disease, Rossy PSP Centre and the Morton and Gloria Shulman Movement Disorders Clinic Toronto Western Hospital Toronto Ontario Canada

2. Instituto de Neurociencia Cognitiva y Traslacional INECO‐Favaloro‐CONICET Buenos Aires Argentina

3. Department of Human Neuroscience Sapienza University Rome Italy

4. Molecular Neurosciences, Developmental Neurosciences, Zayed Centre for Research into Rare Disease in Children UCL Great Ormond Street Institute of Child Health London United Kingdom

5. Department of Neurology Great Ormond Street Hospital London United Kingdom

6. Departments of Neurosciences and Pediatrics University of California San Diego San Diego California USA

7. Division of Neurology, Rady Children's Hospital; Rady Children's Institute for Genomic Medicine San Diego California USA

8. Division of Neurology, Pediatric Deep Brain Stimulation Program Movement Disorder and Neuromodulation Program at the Hospital for Sick Children Toronto Ontario Canada

9. Department of Pediatrics University of Toronto Toronto Ontario Canada

10. Tanz Centre for Research in Neurodegenerative Disease University of Toronto Toronto Ontario Canada

11. Department of Medicine, Division of Neurology University Health Network and the University of Toronto Toronto Ontario Canada

Abstract

AbstractAcute presentation of severe motor disorders is a diagnostic and management challenge. We define severe acute motor exacerbations (SAME) as acute/subacute motor symptoms that persist for hours‐to‐days with a severity that compromise vital signs (temperature, breath, and heart rate) and bulbar function (swallowing/dysphagia). Phenomenology includes dystonia, choreoathetosis, combined movement disorders, weakness, and hemiplegic attacks. SAME can develop in diverse diseases and can be preceded by triggers or catabolic states. Recent descriptions of SAME in complex neurodevelopmental and epileptic encephalopathies have broadened appreciation of this presentation beyond inborn errors of metabolism. A high degree of clinical suspicion is required to identify appropriately targeted investigations and management. We conducted a comprehensive literature analysis of etiologies. Reported triggers are described and classified as per pathophysiological mechanism. A video of six cases displaying multiple SAME with diverse outcomes is provided. We identified 50 different conditions that manifest SAME, some associated with developmental regression. Etiologies include disorders of metabolism: energy substrate, amino acids, complex molecules, vitamins/cofactors, minerals, and neurotransmitters/synaptic vesicle cycling. Non‐metabolic neurodegenerative and genetic disorders that present with movement disorders and epilepsy can additionally manifest SAME. A limited number of triggers are grouped here, together with an approach to investigations and general management strategies. Several neurogenetic and neurometabolic disorders manifest SAME. Identifying triggers can help in certain cases narrow the differential diagnosis and guide the expeditious application of targeted therapies to minimize adverse developmental and neurological consequences. This process may inform pathogenesis and eventually improve our understanding of the mechanisms that lead to the development of SAME. © 2024 International Parkinson and Movement Disorder Society.

Publisher

Wiley

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