| Literature DB >> 25684057 |
Guy Helman1, Keith Van Haren2, Joshua L Bonkowsky3, Genevieve Bernard4, Amy Pizzino2, Nancy Braverman5, Dean Suhr6, Marc C Patterson7, S Ali Fatemi8, Jeff Leonard9, Marjo S van der Knaap10, Stephen A Back11, Stephen Damiani12, Steven A Goldman13, Asako Takanohashi14, Magdalena Petryniak15, David Rowitch16, Albee Messing17, Lawrence Wrabetz18, Raphael Schiffmann19, Florian Eichler20, Maria L Escolar21, Adeline Vanderver22.
Abstract
Leukodystrophies are a heterogeneous, often progressive group of disorders manifesting a wide range of symptoms and complications. Most of these disorders have historically had no etiologic or disease specific therapeutic approaches. Recently, a greater understanding of the pathologic mechanisms associated with leukodystrophies has allowed clinicians and researchers to prioritize treatment strategies and advance research in therapies for specific disorders, some of which are on the verge of pilot or Phase I/II clinical trials. This shifts the care of leukodystrophy patients from the management of the complex array of symptoms and sequelae alone to targeted therapeutics. The unmet needs of leukodystrophy patients still remain an overwhelming burden. While the overwhelming consensus is that these disorders collectively are symptomatically treatable, leukodystrophy patients are in need of advanced therapies and if possible, a cure.Entities:
Keywords: Care; Consensus; Leukodystrophy; Outcomes; Prevention; Therapy
Mesh:
Year: 2015 PMID: 25684057 PMCID: PMC4390468 DOI: 10.1016/j.ymgme.2015.01.014
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797