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Gait abnormalities are frequently reported in autism. The empirical literature, however, is characterized by inconsistent findings concerning which aspects of gait are affected. We conducted a meta-analysis to summarize study findings that examined temporal and spatial (i.e., two-dimensional) gait parameters in pediatric and adult samples comprising individuals with autism and healthy controls. After searching electronic databases, a total of 18 studies were identified and included in this review. Results from the meta-analyses revealed autism is associated with a wider step width, slower walking speed, longer gait cycle, longer stance time and longer step time. Additionally, autism appears to be associated with greater intra-individual variability on measures of stride length, stride time and walking speed. Meta-regression analyses revealed cadence and gait cycle duration differences, between autism and control groups, become more pronounced with age. Overall, this review demonstrates that autism is associated with gait abnormalities. However, assessment of the methodological quality of the studies reveal, additional research is required to understand the extent that gait abnormalities are specifically linked to autism, or whether they may be secondary to other factors commonly found in this group, such as increased weight. LAY SUMMARY: It is often noted by clinicians that individuals with autism have an awkward or unusual walking style, which is also referred to as gait. In this report, we reviewed past studies that compared gait in individuals with and without autism. Our review indicates autism is associated with an abnormal gait. However, it is not yet clear whether gait abnormalities are caused by autism, or arise due to other factors such as heavier weight, which often co-occurs in this group.
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http://dx.doi.org/10.1002/aur.2443 | DOI Listing |
Biol Open
September 2025
Departments of Biochemistry & Medical Genetics, University of Manitoba, Winnipeg, R3T 2N2, Canada.
The GM2 gangliosidoses are lysosomal storage disorders exhibiting a spectrum of neurological phenotypes ranging from childhood death to debilitating adult-onset neurological impairment. To date, no mouse model harbouring a specific human mutation causing GM2 gangliosidosis has been created. We used CRISPR/Cas9 to generate knockin (KI) mice with the common adult-onset Hexa Gly269Ser variant as well as knockout (KO) mice with Hexa mutations expected to cause complete HexA deficiency.
View Article and Find Full Text PDFJ Mol Neurosci
September 2025
Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI, USA.
Collagen type XX alpha 1 (COL20A1) was recently found to be highly concentrated in perisynaptic Schwann cells (PSCs), the synaptic glia of the neuromuscular junction (NMJ), suggesting that COL20A1 plays important roles in PSCs and at the NMJ. To investigate this possibility, we generated mice lacking Col20a1 only in Schwann cells (Col20a1-SCKO) and globally (Col20a1-gKO). PSCs and NMJs were morphologically unchanged in adult Col20a1-SCKO mice despite these conditional mice exhibiting gait abnormalities.
View Article and Find Full Text PDFBMC Neurol
September 2025
Department of Neurology, Asahi General Hospital, 1326 I, Asahi, Chiba 289-2511, Japan.
Background: Spinocerebellar ataxia type 8 (SCA8) is a rare neurodegenerative disease that is caused by CAG/CTG repeat expansion in the overlapping ATXN8 and ATXN8OS genes and basically entails slowly progressive cerebellar dysfunction with resultant dysarthria, limb incoordination, and gait instability. Moreover, patients with SCA8 may also exhibit pyramidal and extrapyramidal signs, cognitive decline, and involuntary movements. Although SCA8 is an autosomal dominant inheritance disorder, it sometimes seems to be sporadic because of reduced penetrance.
View Article and Find Full Text PDFTrials
August 2025
College of Physical Education and Health, Guangxi Normal University, Guilin, China.
Background: Total knee arthroplasty has proven to be an effective method for treating severe osteoarthritis, but this procedure may induce abnormal symptoms of gait and muscle synergy after surgery. Motor imagery is a special means of training that can heighten cortical-spinal excitability and spinal transmission efficiency. The training method can fortify muscle strength, enhance joint range of motion, and ameliorate gait and muscle synergy control patterns, all while avoiding postoperative intense pain resulting from high-intensity exercise.
View Article and Find Full Text PDFJ Biomed Sci
August 2025
State Key Laboratory of Reproductive Medicine and Offspring Health (Suzhou Centre), Suzhou Municipal Hospital, Gusu School, Suzhou Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Suzhou, 215002, China.
Background: Growing evidence highlights the importance of epitranscriptomic regulation in cerebellar development and function, especially through mA methylation. Nevertheless, the precise function of the RNA demethylase Fto in the cerebellum is still uncertain.
Methods: An Fto knockout (Fto) mouse model was generated to investigate the role of Fto in cerebellar development.