2022
DOI: 10.3389/fnhum.2022.918918
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Comparison of Treadmill Gait Between a Pediatric-Aged Individual With SYNGAP1-Related Intellectual Disability and a Fraternal Twin

Abstract: SYNGAP1-related Intellectual Disability (SYNGAP1-ID) is a rare neurodevelopmental condition characterized by profound intellectual disability, gross motor delays, and behavioral issues. Ataxia and gait difficulties are often observed but have not yet been characterized by laboratory-based kinematic analyses. This investigation identified gait characteristics of an individual with SYNGAP1-ID and compared these with a neurotypical fraternal twin. Lower limb kinematics were collected with a 12-camera motion captu… Show more

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Cited by 4 publications
(3 citation statements)
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References 20 publications
(30 reference statements)
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“…SYNGAP1-related intellectual disability, or SYNGAP1-related developmental and epileptic encephalopathy (SYNGAP1-DEE, OMIM 612621), typically presents with early life developmental delays without frank regression, in association with exam findings including hypotonia or strabismus (106). In addition-and similar to Phelan McDermid-one observed symptom (and possible biomarker) is ataxic/wide-based gait, again possibly suggestive of cerebellar dysfunction and implicating cerebro-cerebellar networks, which affects over 50% of cases (107). Some of these phenotypic traits had, previously, led to inclusion of SYNGAP1-DEE patients in the category of "Angelman-like" syndrome (108).…”
Section: Syngap1-developmental and Epileptic Encephalopathymentioning
confidence: 71%
“…SYNGAP1-related intellectual disability, or SYNGAP1-related developmental and epileptic encephalopathy (SYNGAP1-DEE, OMIM 612621), typically presents with early life developmental delays without frank regression, in association with exam findings including hypotonia or strabismus (106). In addition-and similar to Phelan McDermid-one observed symptom (and possible biomarker) is ataxic/wide-based gait, again possibly suggestive of cerebellar dysfunction and implicating cerebro-cerebellar networks, which affects over 50% of cases (107). Some of these phenotypic traits had, previously, led to inclusion of SYNGAP1-DEE patients in the category of "Angelman-like" syndrome (108).…”
Section: Syngap1-developmental and Epileptic Encephalopathymentioning
confidence: 71%
“…Numerous research studies have applied statistical techniques such as statistical parametric mapping (SPM) and symmetry indices to examine interlimb asymmetries in individuals with pathology. These investigations employ the average disparity between the left and right limbs as a measure to evaluate symmetry [ 4 , 5 , 10 , 23 , 30 , 31 ]. However, there is a notable absence of studies applying these methods to establish the baseline level of asymmetry in information for healthy individuals during overground walking.…”
Section: Introductionmentioning
confidence: 99%
“…These questions were addressed through the use of zero-dimensional (traditional kinematic and electromyographic measures) and one-dimensional (utilizing statistical parametric mapping) analyses. Previous use of these methods has been found to provide complementary information that was not otherwise apparent given use of only one or the other ( Layne et al, 2022a ; Layne et al, 2022b ).…”
Section: Introductionmentioning
confidence: 99%