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Atypical activation during the Embedded Figures Task has been demonstrated in autism, but has not been investigated in siblings or related to measures of clinical severity. We identified atypical activation during the Embedded Figures Task in participants with autism and unaffected siblings compared with control subjects in a number of temporal and frontal brain regions. Autism and sibling groups, however, did not differ in terms of activation during this task. This suggests that the pattern of atypical activation identified may represent a functional endophenotype of autism, related to familial risk for the condition shared between individuals with autism and their siblings. We also found that reduced activation in autism relative to control subjects in regions including associative visual and face processing areas was strongly correlated with the clinical severity of impairments in reciprocal social interaction. Behavioural performance was intact in autism and sibling groups. Results are discussed in terms of atypical information processing styles or of increased activation in temporal and frontal regions in autism and the broader phenotype. By separating the aspects of atypical activation as markers of familial risk for the condition from those that are autism-specific, our findings offer new insight into the factors that might cause the expression of autism in families, affecting some children but not others.
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http://dx.doi.org/10.1093/brain/aws229 | DOI Listing |
J Physiol
September 2025
Departamento de Neurofisiología, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, México City, México.
At chemical synapses, the interplay between the stimulation pattern, the dynamics of presynaptic calcium concentration and the use and replenishment of the vesicle pool causes plasticity phenomena such as synaptic facilitation and depression. These phenomena may coexist, with their relative contribution depending mostly on the initial release probability. Synaptic facilitation is caused by an increased probability of release as a result of presynaptic calcium accumulation, whereas synaptic depression is attributed to depletion of the releasable vesicle pool.
View Article and Find Full Text PDFFront Oncol
August 2025
Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Introduction: Synovial sarcoma (SS) is one of the most prevalent malignant soft tissue sarcomas in children and adolescents. Pediatric populations often present with atypical features, complicating the differentiation from benign intramuscular venous malformations (VMs).
case Presentation: An 11-year-old male with a four-year history of progressive right plantar pain and a compressible intramuscular mass.
Indian J Nucl Med
August 2025
Department of Nuclear Medicine, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi, China.
This case demonstrates extraosseous technetium-99m methylene diphosphonate (Tc-99m MDP) accumulation from an atypical ossifying fibromyxoid tumor (OFMT). A 63-year-old man presented with a 10-year history of a gradually enlarging, painless back mass. Physical examination revealed multiple hard, nontender subcutaneous nodules without signs of inflammation or pigmentation.
View Article and Find Full Text PDFIndian J Nucl Med
August 2025
Department of Nuclear Medicine, Jawaharlal Institute of Postgraduate Medical Education Research, Puducherry, India.
We present a unique case of a heart-shaped lesion identified on Fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) imaging in a patient with metastatic adenocarcinoma of the left lung. The patient, initially diagnosed with a mass in the left upper lobe and a lytic lesion in the L3 vertebra, underwent chemoradiation therapy. Subsequent imaging revealed significant metabolic activity reduction in lung and vertebral lesions.
View Article and Find Full Text PDFHematol Transfus Cell Ther
September 2025
Department of Medicine, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada; Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON, Canada; Department of Oncology, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada; Th
Background: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening immune disorder characterized by excessive inflammation and multiorgan involvement. Rarely, HLH can manifest with signs and symptoms isolated to the central nervous system (CNS). This case report highlights the unique clinical course of CNS-isolated HLH in a 19-year-old female who, despite a nine-year delay in diagnosis, achieved disease remission following a hematopoietic stem cell transplant (HSCT).
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