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pam and then transferred to a tertiary children’s hospital. On physical examination, there was facial grimacing and prominent choreoathetoid move- ments in bilateral upper and lower extremities. There was absence of rigidity, lip smacking/puck- ering, cog wheeling, dystonia, and hyperreflexia. The mother reported the patient had a long his- tory of recurrent streptococcal infections includ- ing a confirmed streptococcal infection several months prior to this admission, which was treat- ed with a 10-day course of amoxicillin. The MRI was unremarkable, and the EEG showed mild slowing. Laboratory findings were remarkable only for elevated creatine kinase 661 (4-87 U/L) and mildly elevated CRP 22.8 (0.0-10.0 mg/L). His rapid antigen streptococcal test (RAST), ASO titre (< 25), and ADB titre (<86) were negative. WE-D from decreasing quetiapine dose and/ or a movement disorder complicated by PAN- DAS is a plausible explanation of the patient’s abnormal movements. Sydenham’s Chorea is also high on the differential. Treatment was ini- tiated by increasing quetiapine up to 200 mg PO BID, which led to gradual improvement of ab- normal movements. A trial of antibiotic therapy was recommended by the psychiatry consults Table team; however, patient showed objective signs of improvement with quetiapine titration alone. At an outpatient three-month follow up visit, re- cords indicate that the patient is stable on the quetiapine without any abnormal movements. current or post-streptococcal infection. These movements could be understood as either PAN- DAS, SC, or WE-D or a combination of all three conditions. Both patients responded to increasing doses of quetiapine. We hypothesize that the sud- den onset of these three rare conditions resulted from the reduction of antipsychotics in the con- text of post-streptococcal infection, leading to a severe PANDAS syndrome. The clinical implica- tion is that clinicians should consider prophylactic treatment with antibiotics for complex psychiatric syndromes with recurrent strep infection, take caution in reducing antipsychotics in this popu- lation, and that the presentation of SC may be a manifestation of a PANDAS syndrome. References 1. in clinical neurology. 1984;4:229-60. 2. Klawans HL, Brandabur MM. Chorea in child- hood. Pediatric annals. 1993;22(1):41-50. 3. Gardos G, Cole JO, Tarsy D. Withdrawal syn- dromes associated with antipsychotic drugs. Am J Psychiatry. 1978;135(11):1321-4. 4. Swedo S, Leckman J, Rose N. From research subgroup to clinical syndrome: modifying the PANDAS criteria to describe PANS (pediatric acute-onset neuropsychiatric syndrome). Pediatr Therapeut. 2012;2(2):113. 5. Toufexis MD, Hommer R, Gerardi DM, Grant P, Rothschild L, D'Souza P, et al. Disordered eat- ing and food restrictions in children with PAN- DAS/PANS. J Child Adolesc Psychopharmacol. Discussion It is postulated that neuro inflammation plays a major role in the etiology and pathogenesis of PANDAS. 6 Serum IgG from patients with SC and PANDAS, which bind to components of the group A Streptococcus cell wall, have also been shown to cross-react with neuronal components in the basal ganglia caudate, putamen, and the globus pallidus. 7 The PANDAS Consortium recommends conventional psychiatric treatment 7 and targeted antimicrobial therapy 8 for severe infections resis- tant to antibiotic therapy IVIG and corticosteroids. 6 Fahn S. The tardive dyskinesias. Recent advances 2015;25(1):48-56. 6. Jennifer F, Susan S, Tanya M, C. DR, Dritan A, Kyle W, et al. Clinical Management of Pediatric Acute-Onset Neuropsychiatric Syndrome: Part II—Use of Immunomodulatory Therapies. Jour- nal of Child and Adolescent Psychopharmacolo- gy. 2017;27(7):574-93. 7. Kirvan CA, Swedo SE, Kurahara D, Cunningham MW. Streptococcal mimicry and antibody-medi- ated cell signaling in the pathogenesis of Syden- ham's chorea. Autoimmunity. 2006;39(1):21-9. 8. Margo T, Tanya M, James L, Richard S, Kyle W, Cynthia K, et al. Clinical Management of Pediat- Both cases involved patients with a long history of complex and comorbid psychiatric diagnoses treated with multiple medications and changing doses of medications along with a concomitant history of recurrent streptococcal infections. In both cases, changes to the dose of antipsy- chotic, which had never been problematic pre- viously, was followed by SC and PANDAS when the decrease in antipsychotic occurred during Volume 116 • Number 10 ric Acute-Onset Neuropsychiatric Syndrome: Part I—Psychiatric and Behavioral Interventions. Journal of Child and Adolescent Psychopharma- cology. 2017;27(7):566-73. April 2020 • 229