Treatment‐resistant schizophrenia with 22q11.2 deletion and additional genetic defects

Treatment‐resistant schizophrenia with 22q11.2 deletion and additional genetic defects

Abstract We report a case of a 61‐year‐old female with 22q11.2 deletion syndrome (22q11.2DS) and a novel heterozygous nonsense variant in MAP1A, identified through whole‐genome sequencing (WGS). The patient presented with intellectual developmental disorder, treatment‐resistant schizophrenia (SCZ),...

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Bibliographic Details
Main Authors: Sawako Furukawa, Shusei Arafuka, Hidekazu Kato, Tomoo Ogi, Norio Ozaki, Masashi Ikeda, Itaru Kushima
Format: Article
Language:English
Published: Wiley 2024-12-01
Series:Neuropsychopharmacology Reports
Subjects:
22q11.2 deletion syndrome
genetics: Human
schizophrenia: Clinical
treatment‐resistant schizophrenia
whole‐genome sequencing
Online Access:https://doi.org/10.1002/npr2.12477
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https://doi.org/10.1002/npr2.12477

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