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Characterization of Fine Motor and Visual Motor Skills in Aicardi-Goutières Syndrome.
Cusack, Stacy V; Gavazzi, Francesco; de Barcelos, Isabella Peixoto; Modesti, Nicholson B; Woidill, Sarah; Formanowski, Brielle; DeMauro, Sara B; Lorch, Scott; Vincent, Ariel; Jawad, Abbas F; Estilow, Timothy; Glanzman, Allan M; Vanderver, Adeline; Adang, Laura A.
Affiliation
  • Cusack SV; Department of Occupational Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Gavazzi F; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • de Barcelos IP; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Modesti NB; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Woidill S; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Formanowski B; Department of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • DeMauro SB; Department of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Lorch S; Department of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Vincent A; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Jawad AF; Division of General Peds, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Estilow T; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Glanzman AM; Department of Occupational Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Vanderver A; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Adang LA; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
J Child Neurol ; 39(3-4): 147-154, 2024 Mar.
Article de En | MEDLINE | ID: mdl-38532733
ABSTRACT
Aicardi-Goutières syndrome is a genetic inflammatory disorder resulting in dispersed neurologic dysfunction. Despite a recognition of overall motor impairment, fine and visual motor skills are undercharacterized. We hypothesize that there is a spectrum of fine and visual motor skills in the Aicardi-Goutières syndrome population as captured by a standard outcome measure, the Peabody Developmental Motor Scales (PDMS-2), which will be proportional to overall disease severity.In a cohort of 74 subjects, the Peabody Developmental Motor Scales-2 grasping and visual-motor integration subtests were administered concurrently with the Aicardi-Goutières syndrome Severity Scale (severe [range 0-3], moderate [range 4-8], and attenuated [range 9-11]). The cohort was also compared by genotype and performance as defined by raw scores. The distribution of Peabody Developmental Motor Scales-2 scores within a genotype was assessed by interquartile ranges (IQRs).Peabody Developmental Motor Scales-2 grasping and visual-motor integration performance was the least variable in the TREX1-cohort (IQR 10.00-12.00) versus the SAMHD1 and IFIH1 cohorts (IQR 51.00-132.00 and 48.50-134.00, respectively). Neurologic severity highly correlated with both fine and visual motor skills (Spearman correlation r = 0.87, 0.91, respectively). A floor effect (lowest 10% of possible scores) was observed within the severe cohort (n = 32/35), whereas a ceiling effect (top 10%) was observed in the attenuated cohort (n = 13/17).This study characterized the spectrum of fine and visual motor function in the Aicardi-Goutières syndrome population, which correlated with overall neurologic dysfunction. The Peabody Developmental Motor Scales-2 grasping and visual-motor integration showed promise as potential assessment tools in moderate and attenuated Aicardi-Goutières syndrome cohorts. A better understanding of fine and visual motor function in this population will benefit clinical care and clinical trial design.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies auto-immunes du système nerveux / Aptitudes motrices / Malformations du système nerveux Limites: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Langue: En Journal: J Child Neurol Sujet du journal: NEUROLOGIA / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies auto-immunes du système nerveux / Aptitudes motrices / Malformations du système nerveux Limites: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Langue: En Journal: J Child Neurol Sujet du journal: NEUROLOGIA / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
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