Catatonia revealing a Fahr syndrome.

J Neurosci Rural Pract

Department of Psychiatry, Ibn Alhassan Hospital, University Hospital of Fez, Fez, Morocco.

Published: March 2023

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174117PMC
http://dx.doi.org/10.25259/JNRP_19_2023DOI Listing

Publication Analysis

Top Keywords

catatonia revealing
4
revealing fahr
4
fahr syndrome
4
catatonia
1
fahr
1
syndrome
1

Similar Publications

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis stands as the most prevalent form of autoimmune encephalitis, primarily affecting young patients and exhibiting a higher incidence among females. Patients frequently present with psychiatric symptoms or cognitive impairments such as speech disturbances, decreased level of consciousness, autonomic dysfunction, as well as seizures, dyskinesias, and catatonia due to overactivation of extrasynaptic NMDA receptors. To date, there is no gold standard for the diagnosis of catatonia; however, a few rating scales exist to measure this phenomenon, with the Bush Francis Catatonia Rating Scale being the most commonly used due to its validity, reliability, and ease of application.

View Article and Find Full Text PDF

The differential diagnosis of neurocognitive and psychiatric disorders, particularly when symptoms overlap significantly, poses a substantial challenge in clinical practice. Parkinson's disease (PD), Lewy body dementia, and catatonia are distinct conditions that can present with similar motor and cognitive symptoms, complicating accurate diagnosis and effective treatment. We report the case of a 45-year-old male patient who presented for electroconvulsive therapy (ECT) evaluation.

View Article and Find Full Text PDF
Article Synopsis
  • - Cerebral brain abscesses are rare but serious, especially in immunocompromised people, and can often imitate psychiatric disorders, complicating their diagnosis.
  • - A case study involves a 47-year-old HIV-positive woman with a psychiatric history who showed unusual symptoms like catatonia, leading to a diagnosis of a large brain abscess after imaging revealed significant issues.
  • - The patient received immediate treatment, including surgery, and showed improvement, highlighting the need for thorough diagnostic procedures and multidisciplinary care in similar cases to ensure better health outcomes.
View Article and Find Full Text PDF
Article Synopsis
  • SHANK1 is a gene that produces a protein involved in the structure and function of excitatory synapses, part of a family that includes SHANK2 and SHANK3.
  • An 11-year-old boy with developmental delays and no family psychiatric history developed catatonia, with imaging and autoimmune tests showing no abnormalities.
  • Genetic testing identified a new, likely harmful SHANK1 variant, marking the first documented case of catatonia linked to a SHANK1 mutation, although similar symptoms have been associated with SHANK3 issues.
View Article and Find Full Text PDF

Evaluating catatonia care in the psychiatric emergency room: A retrospective study.

J Psychiatr Res

December 2024

Department of Psychiatry and Behavioral Health, Stony Brook University Renaissance School of Medicine, 101 Nicolls Road, Stony Brook, NY, 11794, USA. Electronic address:

Background: Catatonia, characterized by motor, affective, and speech disturbances, is a prevalent yet frequently misdiagnosed syndrome in the psychiatric domain, with reported prevalence ranging from 5% to 18%. This study aimed to ascertain the incidence of catatonia diagnoses and the quality of care provided within the psychiatric emergency room (ER), while also evaluating psychiatrists' general awareness of the syndrome through a survey.

Methods: A retrospective analysis of psychiatric ER records spanning June 18th to August 20th, 2022, was conducted to assess catatonia diagnosis frequency and treatment approaches.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!