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3.
Asian J Psychiatr ; 69: 103004, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35016069

RESUMO

Catatonia has been reported as one among many neuropsychiatric manifestations associated with COVID-19 infection. Catatonia and COVID-19 co-occurrence remain clinical concerns, often posing challenges pertaining to diagnosis, and especially management. Limited information is available regarding the appropriate approaches to the management of catatonia in COVID-19 infection, particularly with reference to the safety and efficacy of benzodiazepines and Electro-convulsive therapy (ECT). We present our experience of five patients with catatonia consequent to heterogeneous underlying causes and concurrent COVID-19 infection, who received care at the psychiatric COVID unit of our tertiary care psychiatric hospital. An interesting observation included varying underlying causes for catatonia and the potential role that COVID-19 infection may have played in the manifestation of catatonia. In our experience, new-onset catatonia with or without pre-existing psychiatric illness and concurrent COVID-19 can be safely and effectively managed with lorazepam and/or ECTs. However, critical to the same is the need to implement modified protocols that integrate pre-emptive evaluation for COVID-19 disease and proactive monitoring of its relevant clinical parameters, thereby permitting judicious and timely implementation of catatonia-specific treatment options.


Assuntos
COVID-19 , Catatonia , Eletroconvulsoterapia , Catatonia/diagnóstico , Catatonia/etiologia , Catatonia/terapia , Hospitais Psiquiátricos , Humanos , SARS-CoV-2 , Atenção Terciária à Saúde
4.
Parkinsonism Relat Disord ; 90: 49-51, 2021 09.
Artigo em Inglês | MEDLINE | ID: mdl-34365112

RESUMO

PLA2G6 gene associated neurodegenerative disorders resulting from homozygous c. 2222G > A (p.Arg741Gln) mutation were detected in two cases having variable neuropsychiatric phenotypic and imaging findings. Exome analysis helped identification of rare alleles, reinforcing ethnographic antecedents to geographical clustering of rare mutations and, essential to understanding biology of neurodegenerative disorders.


Assuntos
Fosfolipases A2 do Grupo VI/genética , Transtornos Heredodegenerativos do Sistema Nervoso/genética , População Branca/genética , Alelos , Variação Biológica da População , Feminino , Transtornos Heredodegenerativos do Sistema Nervoso/etnologia , Homozigoto , Humanos , Índia , Masculino , Ilustração Médica , Mutação , Fenótipo , Sequenciamento do Exoma , Adulto Jovem
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