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Brainstem and vermis atrophy in catatonia.
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The computerized tomographic scans of five catatonic patients and five matched controls were blindly assessed. The catatonic patients showed preponderant atrophy of the brainstem and cerebellar vermis. Catatonia may be associated with lesions in these areas.
Psychological approaches to chronic catatonia-like deterioration in autism spectrum disorders.
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The psychological dysfunctions that may underlie catatonia-like deterioration in autism spectrum disorders are discussed. Clinical observation suggests that an important factor is ongoing stress. The evidence for this from research and clinical observation is considered. The lack of evidence
Catatonia with frontal lobe atrophy.
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A middleaged woman with a four year history of behavioural change including episodes of catatonia is described. Despite a persistently abnormal electroencephalogram, the patient was diagnosed repeatedly as suffering from a primary psychiatric disorder. Neurological examination and psychological
Three patients with mood disorders showing catatonia and frontotemporal lobes atrophy.
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Here we report the cases of three patients with mood disorders showing catatonia and frontotemporal lobe atrophy. Catatonia is a syndrome linked to frontal dysfunction that most frequently occurs in patients with mood disorders. The diagnostic criteria of catatonia and frontotemporal dementia partly
Neurodegenerative and psychiatric overlap in frontotemporal lobar degeneration: a case of familial frontotemporal dementia presenting with catatonia.
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The behavioral variant of frontotemporal dementia (FTD) begins with psychiatric symptoms, including changes in personal conduct and/or interpersonal behavior. Prior to developing cognitive impairment, differentiating FTD from primary psychiatric disorders, like schizophrenia, can be challenging.
Catatonia due to Thalamic Degeneration: A Case Report.
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[Atrophy of the globus pallidus, substancia nigra, and nucleus subthalamicus. Akinetic syndrome with palilalia, oppositional rigidity and catatonia].
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Cerebellar atrophy and catatonia.
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Successful treatment of catatonia in a young man with schizophrenia and progressive diffuse cerebral atrophy.
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Progressive catatonia.
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We present the case of a young man with a diagnosis of a childhood-onset pervasive developmental disorder who developed a progressive neurologic deterioration with persistent catatonia and right hemiparesis. On his initial evaluation approximately three years after the onset of mutism, he manifested
Catatonia - case report and review.
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Catatonia is a neuro-psychiatric disorder that can occur in medical, psychiatric and drug-induced conditions but is often unrecognised. A 64 year-old woman was admitted to hospital for assessment of a significant deterioration in her ability to communicate and function normally so that she had
Triplet repeats in clinical subtypes of schizophrenia: variation at the DRPLA (B 37 CAG repeat) locus is not associated with periodic catatonia.
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Clinical evidence for a dominant mode of inheritance and anticipation in periodic catatonia, a distinct subtype of schizophrenia, indicates that genes with triplet repeat expansions or other unstable repetitive elements affecting gene expression may be involved in the etiology of this disorder.
Electroconvulsive therapy for catatonia in a boy with hydrocephalus and an arachnoid cyst.
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We report on the successful use of electroconvulsive therapy in a 13-year-old boy with congenital hydrocephalus, a history of multiple shunt revisions, and a stable prepontine arachnoid cyst, who experienced profound catatonic deterioration. After initial shunt placement at age 20 months, the
Benzodiazepines in catatonia associated with systemic lupus erythematosus.
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Neuropsychiatric disturbances are found in 50-70% of systemic lupus erythematosus (SLE) patients. However, there are rare cases of catatonia being described in SLE. Some studies have shown the effectiveness of high-dose steroid, plasma exchange and electroconvulsive therapy (ECT) in lupus catatonia.
Early-Onset Alzheimer's Disease Masquerading as Catatonia
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A 35-year-old woman with a history of sexual trauma was brought in by her family for further evaluation of depressive symptoms and progressive decline in activities of daily living. She was admitted to the inpatient psychiatric unit for the treatment of suspected catatonia. After failure to respond
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