Title of article
Dystonic Movement Disorder as Symptom of Catatonia in AutismSpectrum Disorder
Author/Authors
Bravaccio, Carmela Department of Translational Medical Sciences - Child Neuropsychiatry Unit - University Federico II of Naples - Via Sergio Pansini - Naples, Italy , Riccio, Maria Pia Department of Translational Medical Sciences - Child Neuropsychiatry Unit - University Federico II of Naples - Via Sergio Pansini - Naples, Italy , Siracusano, Rosamaria Department of Translational Medical Sciences - Child Neuropsychiatry Unit - University Federico II of Naples - Via Sergio Pansini - Naples, Italy , d’Alessandro, Ilaria Department of Translational Medical Sciences - Child Neuropsychiatry Unit - University Federico II of Naples - Via Sergio Pansini - Naples, Italy , Marino, Maria Department of Translational Medical Sciences - Child Neuropsychiatry Unit - University Federico II of Naples - Via Sergio Pansini - Naples, Italy
Pages
3
From page
1
To page
3
Abstract
Catatonia is increasingly recognized as a comorbid psychiatric condition in autism spectrum disorder (ASD), but theoverlap of behavioral characteristics between these disorders raises many diagnostic challenges. Moreover, recognizing symptomsin ASD patients with medium-low functioning might be difficult. Literature on this argument is poor, especially for children.Casepresentation. We report the case of an ASD patient with low cognitive functioning, who presented a complex symptomatology,characterized by progressive regression with loss of autonomy and involuntary movements that assume“dystonic”features.Organic pathology was excluded, and catatonia, with peculiar dystonic characteristics, was diagnosed. An intervention based onelimination of stressful factors, resumption of routines, and support for parents led to the resolution of catatonic symptoms.Conclusions. The case describes the presence among the catatonic symptoms in ASD of involuntary“dystonic”movements; sofar, little reported in literature; it highlights that the catatonia may present with a broad spectrum of motor abnormalities. Thereis still little evidence for treatment of catatonia and ASD. Our case highlights how it is equally important to take into accounttriggering factors when implementing a nonpharmacological treatment. So, it represents an example of diagnostic andtherapeutic challenges of catatonia in ASD, especially in low functioning forms
Keywords
Dystonic Movement Disorder , Symptom , Catatonia , AutismSpectrum Disorder
Journal title
Case Reports in Psychiatry
Serial Year
2020
Record number
2606267
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