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Case report: Evolution of catatonic mutism and psychotic symptoms in an adolescent with Down syndrome: transition from Down syndrome disintegrative disorder to anti-N-methyl-D-aspartate receptor encephalitis.

Authors :
Minamisawa Y
Sato M
Saito Y
Takeuchi F
Miyazaki H
Odaka M
Yamamoto A
Oyama Y
Watanabe Y
Takeshita S
Takahashi Y
Source :
Frontiers in neurology [Front Neurol] 2023 Jun 09; Vol. 14, pp. 1200541. Date of Electronic Publication: 2023 Jun 09 (Print Publication: 2023).
Publication Year :
2023

Abstract

During her first year of junior high school, a 12-year-old Japanese girl with Down syndrome experienced dizziness, gait disruption, paroxysmal weakness in her hands, and sluggish speaking. Regular blood tests and a brain MRI revealed no abnormalities, and she was tentatively diagnosed with adjustment disorder. Nine months later, the patient experienced a subacute sickness of chest pain, nausea, sleep problem with night terrors, and delusion of observation. Rapid deterioration then developed with simultaneous fever, akinetic mutism, loss of facial expression, and urine incontinence. These catatonic symptoms improved after a few weeks after admission and treatment with lorazepam, escitalopram, and aripiprazole. After discharge, nonetheless, daytime slumber, empty eyes, paradoxical laughter, and declined verbal communication persisted. Upon confirmation of the cerebrospinal N-methyl-D-aspartate (NMDA) receptor autoantibody, methylprednisolone pulse therapy was tried, but it had little effect. Visual hallucinations and cenesthopathy, as well as suicidal thoughts and delusions of death, have predominated in the following years. Cerebrospinal IL-1ra, IL-5, IL-15, CCL5, G-CSF, PDGFbb, and VFGF were raised in the early stage of initial medical attention with nonspecific complaints, but were less prominent in the later stages of catatonic mutism and psychotic symptoms. We suggest a disease concept of progression from Down syndrome disintegrative disorder to NMDA receptor encephalitis, based on this experience.<br />Competing Interests: YT received research grants-in-aid for Scientific Research I nos. 15K09634, 18K07865, and 21K07788; Health and Labor Sciences Research Grants for Comprehensive Research on Disability Health and Welfare, Japan (JPMH20FC1039), lecture fee from Daiichisankyo, Eisai, Nihon Pharma, Eisai China, Ono Pharamaceutical, Novartis, UCB, and an academic donation from Eisai. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Minamisawa, Sato, Saito, Takeuchi, Miyazaki, Odaka, Yamamoto, Oyama, Watanabe, Takeshita and Takahashi.)

Details

Language :
English
ISSN :
1664-2295
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in neurology
Publication Type :
Report
Accession number :
37360353
Full Text :
https://doi.org/10.3389/fneur.2023.1200541