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Descriptive Psychopathology: The Signs and Symptoms of ...

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300 Section 3: Examination domainsparoxysms <strong>of</strong> pr<strong>of</strong>anity, affects a third <strong>of</strong> patients. Echolalia <strong>and</strong> echopraxia occurin one-third <strong>of</strong> patients. 56Behavioral disturbances including hyperactivity <strong>and</strong> attentional <strong>and</strong> othercognitive problems, school <strong>and</strong> social difficulties, classroom disruption, fighting,temper tantrums, <strong>and</strong> mood swings are reported in half <strong>of</strong> GTS sufferers. <strong>The</strong>pattern may lead to the mistaken diagnosis <strong>of</strong> manic-depression. A small proportion<strong>of</strong> GTS patients meet criteria for antisocial personality disorder, exhibitsexually inappropriate behavior (e.g. compulsively groping or commenting), areaggressive <strong>and</strong> assaultive, <strong>and</strong> cruel to animals <strong>and</strong> peers. Phobias occur in 20%<strong>of</strong> GTS patients.Sleep disturbances are common in patients with GTS, <strong>and</strong> include initialinsomnia, talking during sleep, nightmares <strong>and</strong> night terrors, somnambulism(sleep walking), <strong>and</strong> bruxism (teeth grinding). Up to a third are enuretic.Pediatric autoimmune neuropsychiatric disorder associatedwith Streptococcus infection (PANDAS) 57Beta-hemolytic streptococcal A infection may be associated in the followingtwo months with the rapid emergence <strong>of</strong> PANDAS, particularly in patients whoearly on in the infection develop chorea or tics. Boys aged 6–7 years, <strong>of</strong>ten with afamily history <strong>of</strong> autoimmune disease (e.g. Grave’s disease, rheumatoid arthritis)are most <strong>of</strong>ten affected. <strong>Symptoms</strong> include GTS features, Sydenham’s chorea,squirming <strong>and</strong> fidgeting that can be mistaken for ADHD, anorexia nervosa, <strong>and</strong>mood disturbances. High levels <strong>of</strong> antineuronal antibodies leading to striatalinflammation <strong>and</strong> the MRI finding <strong>of</strong> enlarged striatal volumes confirm thediagnosis. While most patients fully recover, some become chronically ill, asillustrated by Patient 12.1.Patient 12.1A 17-year-old boy with a history <strong>of</strong> Asperger’s syndrome <strong>and</strong> migraine waspsychiatrically hospitalized because <strong>of</strong> worsening OCD symptoms <strong>and</strong> thedevelopment <strong>of</strong> catatonia. He recently stopped eating, losing 15 lbs in thetwo weeks prior to admission. He spent hours ritually touching certain objectsin a certain sequence. He stood for long periods staring. He stopped doing hisschool work <strong>and</strong> engaging in his interests. He complained <strong>of</strong> his migraineheadaches worsening during this period.On admission, his muscle tone was increased <strong>and</strong> he could be postured,briefly retaining the new position. He exhibited automatic obedience <strong>and</strong>Gegenhalten. His speech was minimal, prosectic <strong>and</strong> he had echolalia. Lorazepamdid not relieve his catatonia. He received 19 bilateral ECT which didrelieve the catatonia, <strong>and</strong> he was discharged on valproic acid <strong>and</strong> alprazolam. 58

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