Five affected siblings were referred with a probable diagnosis of proximal adult-type spinal muscular atrophy (SMA) based on lower motor neuron signs (muscle weakness and atrophy, hypotony, hypoactive or absent reflexes, and fasciculations), normal or borderline serum creatine kinase levels, and a neurogenic pattern on electromyography, compatible with motor neuron disease, in one patient. No exon 7-8 deletion in the survival motor neuron (SMN) gene was found. Linkage analysis excluded the SMN and all known autosomal recessive limb girdle muscular dystrophy loci, with the exception of LGMD-2A. A homozygous R769Q mutation in the calpain-3 gene and absence of muscle calpain-3 protein confirmed a calpainopathy. This family suggests that the clinical spectrum of calpainopathy might be broader and that this diagnosis might be considered in patients with an atypical motor neuron disease.
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http://dx.doi.org/10.1385/jmn:21:3:233 | DOI Listing |
Science
January 2025
Department of Medicine and Surgery, University of Parma, Parma, Italy.
The current understanding of primate natural action organization derives from laboratory experiments in restrained contexts (RCs) under the assumption that this knowledge generalizes to freely moving contexts (FMCs). In this work, we developed a neurobehavioral platform to enable wireless recording of the same premotor neurons in both RCs and FMCs. Neurons often encoded the same hand and mouth actions differently in RCs and FMCs.
View Article and Find Full Text PDFThe NSD-ISS Working Group developed a data-driven approach to: 1) determine a biologic definition for disease; 2) establish a framework for a disease staging platform. NSD is defined by the presence of pathologic n-asyn (S) assessed by a validated in vivo biomarker and ultimate presence of dopaminergic neuronal dysfunction (D). This biologic definition is independent of the presence of clinical features, or if present, of the specific clinical syndrome.
View Article and Find Full Text PDFBackground: Preclinical Alzheimer's disease research has gained traction as a potential point of intervention, though it is relatively unknown how early stages of the disease impact cortical health. The following study utilizes optical imaging methods (Figure 1) to characterize changes in neuronal, glutamate, and hemodynamic activities in a preclinical amyloidosis mouse model of the disease.
Method: Five (n = 5; 2 females & 3 males) APPswe/PS1dE9 x Thy1-jRGECO1a double transgenic mice were breed for whole-brain fluorescent imaging of neuronal activity.
Alzheimers Dement
December 2024
Radboud University Medical Center, Nijmegen, Gelderland, Netherlands.
Background: Commissural tracts are the white matter fibre bundles intercommunicating left and right brain hemispheres. They integrate many cognitive functions such as memory, verbal processing, motor and perceptual skills. Also, commissures connect specific layers of cortical neurons that are also lost in Alzheimer's disease (AD) and other neurodegenerative disorders.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
National Institutes of Health, Bethesda, MD, USA.
Background: Detecting changes in perivascular spaces (PVS) holds promise as a biomarker for neurodegenerative diseases. These spaces exhibit increased protein accumulation and dilatation in neurodegenerative diseases even preceding symptomatic stages. Advanced MRI techniques at high fields offer unparalleled clarity in visualizing these subtle structures.
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