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CASE REPORT
Year : 2020  |  Volume : 25  |  Issue : 1  |  Page : 60-62

Catatonia in a young woman with intellectual disability and vitamin D deficiency managed with electroconvulsive therapy


Department of Psychiatry, Postgraduate Institute of Medical Education and Research, Chandigarh, India

Correspondence Address:
Sandeep Grover
Department of Psychiatry, Post Graduate Institute of Medical Education and Research, Chandigarh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jmhhb.jmhhb_22_20

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Catatonia as a syndrome is known to be associated with multiple psychiatric and medical conditions. Although catatonia has been reported in patients with neurodevelopmental disorders such as autism, there is lack of literature on catatonia in subjects with intellectual disability, especially among the adults. In terms of nutritional deficiencies, catatonia has rarely been reported to be associated with Vitamin D deficiency. In this report, we report a 20-year-old female who presented with catatonia in the absence of evidence of any other psychiatric disorders. Physical examination and investigations did not reveal evidence of any other abnormality, except for Vitamin D deficiency. However, the patient required treatment with electroconvulsive therapy for the management of catatonic symptoms followed by olanzapine up to 7.5 mg for managing psychotic symptoms on follow-up.


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