Abstract | BACKGROUND: CASE PRESENTATION: We present the case of a 40-year-old female patient diagnosed with TRS and 22q11.2DS who was effectively treated with clozapine. She was diagnosed with schizophrenia and mild intellectual disability during her adolescence; despite being hospitalized for a period of 10 years beginning in her 30s, she continued to exhibit symptoms of impulsivity, and explosive behavior, requiring periods of isolation. We ultimately decided to switch her medication to clozapine, which was administered with caution and gradually titrated upward, with no discernable adverse effects, resulting in a marked improvement in her symptoms and obviated the need for isolation. Subsequently, the patient's history of congenital heart disease and facial abnormalities prompted initial suspicions of a 22q11.2DS diagnosis, which was subsequently confirmed through genetic testing. CONCLUSION:
Clozapine may serve as an efficacious pharmacological intervention for TRS patients with 22q11.2DS, including those of Asian descent.
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Authors | Arisa Tsurue, Hideki Funahashi, Keiichi Tsurue, Masahiko Kawano, Yasushi Ishida, Yoji Hirano |
Journal | Neuropsychopharmacology reports
(Neuropsychopharmacol Rep)
Vol. 43
Issue 2
Pg. 272-276
(Jun 2023)
ISSN: 2574-173X [Electronic] United States |
PMID | 36929244
(Publication Type: Case Reports)
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Copyright | © 2023 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. |
Chemical References |
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Topics |
- Humans
- Female
- Adolescent
- Adult
- DiGeorge Syndrome
(complications, drug therapy, genetics)
- Schizophrenia
(complications, drug therapy, genetics)
- Clozapine
(therapeutic use)
- Schizophrenia, Treatment-Resistant
- Genetic Testing
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