Results 31 to 40 of about 1,346,685 (174)

Methylphenidate-Induced Oculogyric Crisis in a Patient with Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder: A Case Report

Psychiatry and Clinical Psychopharmacology, 2021
Methylphenidate is one of the agents used in the treatment of attention deficit hyperactivity disorder. In the literature, the following side effects were reported from the use of methylphenidate: sleep and appetite problems, blood pressure and heart ...
Nilfer Sahin, Damla Balkan, Azat Duman
doaj   +1 more source

A case of aripiprazole-associated oculogyric crisis. [PDF]

Dusunen Adam
Cabuk K, Gokcay H.
europepmc   +2 more sources

Oculogyric crisis caused by clozapine： a case report

Sichuan jingshen weisheng, 2022
This paper reported a case of a 14-year-old female patient with schizophrenia of more than 2 years who had poor efficacy on atypical antipsychotics such as aripiprazole， risperidone and olanzapine， and who developed acute dystonia adverse effects during ...
Deng Hongjiang, Zhang Lan
doaj   +1 more source

Tardive Oculogyric Crisis Due to Aripiprazole Treatment in an Adolescent Patient Diagnosed with Bipolar Disorder

Psychiatry and Clinical Psychopharmacology, 2021
Antipsychotics usage in children and adolescents is becoming widespread. One of the extrapyramidal side effects associated with long-term antipsychotic drug use follow-up is an oculogyric crisis (OGC).
Tugce Canol, Sermin Yalin Sapmaz, Aylin Deniz Uzun, Hasan Kandemir   +3 more
doaj   +1 more source

Oculogyric Crisis Due to Low-Dose Olanzapine: A Case Report

, 2021
Objectives: Oculogyric crisis is a dystonic movement disorder characterized by continuous contraction of the ocular muscles and spasmodic movements of the pupils in a fixed position, usually upward.
Ferahkaya, Hursit, Erden, Semih
core   +1 more source

Oculogyric crisis induced by risperidone in a child with GRIN1 variant

Brain Disorders, 2023
The GluN1 subunit of the N-methyl-d-aspartate (NMDA) receptor is encoded by GRIN1 gene. Mutations in this gene can cause neurodevelopmental disorders with or without hyperkinetic movements and seizures.
Ali Mir, Montaha Almudhry, Shahid Bashir, Hamoud Khallaf   +3 more
doaj   +1 more source

Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency

Frontiers in Pediatrics, 2022
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare, neurometabolic disorder resulting from biallelic mutations in the dopa decarboxylase (DDC) gene.
Mohamed O. E. Babiker, Manju A. Kurian, Manju A. Kurian, Jehan Suleiman, Jehan Suleiman   +4 more
doaj   +1 more source

Tardive Oculogyric Dystonia during Concomitant Quetiapine, Fluoxetine and Lithium Therapy: Case Report and Literature Review

Journal of Psychiatry Spectrum, 2022
Oculogyric crisis (OGC) is an acute paroxysmal sustained dystonia that occurs as an adverse drug event, commonly following first-generation antipsychotics and rarely with second-generation antipsychotics.
Ranganath R. Kulkarni, Swapna A. Pandurangi, Raghavendra C. Patil, R. Shantheri Pai   +3 more
doaj   +1 more source

Clozapine Induced Oculogyric Crisis, A Case Report [PDF]

Journal of Mazandaran University of Medical Sciences, 2007
Background and purpose: Oculogyric crisis which is a dystonic reaction commonly caused by typical antipsychotics treatment of acute dystonias, rarely occurs with atypical antipsychotics like clozapine.
E. Salehifar, Pharm.D. , BCPS, S.H. Hosseini, M.D.**   +1 more
doaj  

Eye motor manifestations in children with neurometabolic disorders

Journal of the Formosan Medical Association, 2022
Neurometabolic diseases are complex group of rare neurogenetic disorders, which are difficult to diagnose. Patients may have toxic metabolite accumulation, inadequate energy supply, or neurotransmitter deficiency, resulting in a variety of clinical ...
Hsin-Pei Wang, Lee-Chin Wong, Chia-Jui Hsu, Su-Ching Hu, Yen-Ju Chu, Wang-Tso Lee   +5 more
doaj   +1 more source