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Practical Approaches and Knowledge Gaps in the Care for Children With Leukodystrophies.
Keller, Stephanie R; Mallack, Eric J; Rubin, Jennifer P; Accardo, Jennifer A; Brault, Jennifer A; Corre, Camille S; Elizondo, Camila; Garafola, Jennifer; Jackson-Garcia, April C; Rhee, Jullie; Seeger, Elisa; Shullanberger, Kaprice C; Tourjee, Amanda; Trovato, Melissa K; Waldman, Amy T; Wallace, Jenna L; Wallace, Michael R; Werner, Klaus; White, Angela; Ess, Kevin C; Becker, Catherine; Eichler, Florian S.
Afiliação
  • Keller SR; Department of Pediatrics, Division of Pediatric Neurology, 1371Emory University/Children's Healthcare of Atlanta, Atlanta, GA, USA.
  • Mallack EJ; Department of Pediatrics, Division of Child Neurology, Weill Cornell Medical College/New York-Presbyterian Hospital, New York, NY, USA.
  • Rubin JP; Department of Pediatric Neurology, Northwestern Feinberg School of Medicine, Chicago, IL, USA.
  • Accardo JA; Department of Neurology, Children's Hospital of Richmond at VCU, Richmond, VA, USA.
  • Brault JA; Department of Pediatrics, Division of Pediatric Neurology 5718Vanderbilt University Medical Center, Nashville, TN, USA.
  • Corre CS; Department of Neurology, 2348Massachusetts General Hospital, Boston, MA, USA.
  • Elizondo C; East Boston Neighborhood Health Canter, East Boston, MA, USA.
  • Garafola J; Department of Pediatrics, Division of Pediatric Neurology 5718Vanderbilt University Medical Center, Nashville, TN, USA.
  • Jackson-Garcia AC; 145748Hunter's Hope Foundation, Orchard Park, NY, USA.
  • Rhee J; 233494Children's National Health Systems, Washington, DC, USA.
  • Seeger E; 145748Hunter's Hope Foundation, Orchard Park, NY, USA.
  • Shullanberger KC; 145748Hunter's Hope Foundation, Orchard Park, NY, USA.
  • Tourjee A; Department of Neurology, 2348Massachusetts General Hospital, Boston, MA, USA.
  • Trovato MK; Department of Physical Medicine and Rehabilitation, 20870Kennedy Krieger Institute and Johns Hopkins University, Baltimore, MD, USA.
  • Waldman AT; Division of Neurology, The Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA, USA.
  • Wallace JL; 145748Hunter's Hope Foundation, Orchard Park, NY, USA.
  • Wallace MR; 145748Hunter's Hope Foundation, Orchard Park, NY, USA.
  • Werner K; Department of Pediatrics, 22957Duke University, Durham, NC, USA.
  • White A; Department of Pediatrics, Division of Pediatric Neurology 5718Vanderbilt University Medical Center, Nashville, TN, USA.
  • Ess KC; Department of Pediatrics, Division of Pediatric Neurology 5718Vanderbilt University Medical Center, Nashville, TN, USA.
  • Becker C; Department of Neurology, 2348Massachusetts General Hospital, Boston, MA, USA.
  • Eichler FS; Department of Neurology, 2348Massachusetts General Hospital, Boston, MA, USA.
J Child Neurol ; 36(1): 65-78, 2021 01.
Article em En | MEDLINE | ID: mdl-32875938
ABSTRACT
Leukodystrophies are a group of neurodegenerative genetic disorders that affect approximately 1 in 7500 individuals. Despite therapeutic progress in individual leukodystrophies, guidelines in neurologic care are sparse and consensus among physicians and caregivers remains a challenge. At patient advocacy meetings hosted by Hunter's Hope from 2016-2018, multidisciplinary experts and caregivers met to conduct a literature review, identify knowledge gaps and summarize best practices regarding neurologic care. Stages of severity in leukodystrophies guided recommendations to address different levels of need based on a newly defined system of disease severity. Four core neurologic domains prioritized by families were identified and became the focus of this guideline sleep, pain, seizures/epilepsy, and language/cognition. Based on clinical severity, the following categories were used presymptomatic, early symptomatic, intermediate symptomatic, and advanced symptomatic. Across the leukodystrophies, neurologic care should be tailored to stages of severity while accounting for unique aspects of every disease and multiple knowledge gaps present. Standardized tools and surveys can help guide treatment but should not overburden families.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Desmielinizantes Hereditárias do Sistema Nervoso Central Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Desmielinizantes Hereditárias do Sistema Nervoso Central Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article