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  • Ortigoza-Escobar, J. D. (author)

Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors

  • Article/chapterEnglish2017

Publisher, publication year, extent ...

  • 2017-08-30
  • Wiley,2017

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/259600
  • https://gup.ub.gu.se/publication/259600URI
  • https://doi.org/10.1002/ana.24998DOI

Supplementary language notes

  • Language:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Primary and secondary conditions leading to thiamine deficiency have overlapping features in children, presenting with acute episodes of encephalopathy, bilateral symmetric brain lesions, and high excretion of organic acids that are specific of thiamine-dependent mitochondrial enzymes, mainly lactate, alpha-ketoglutarate, and branched chain keto-acids. Undiagnosed and untreated thiamine deficiencies are often fatal or lead to severe sequelae. Herein, we describe the clinical and genetic characterization of 79 patients with inherited thiamine defects causing encephalopathy in childhood, identifying outcome predictors in patients with pathogenic SLC19A3 variants, the most common genetic etiology. We propose diagnostic criteria that will aid clinicians to establish a faster and accurate diagnosis so that early vitamin supplementation is considered. Ann Neurol 2017;82:317–330. © 2017 American Neurological Association

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Alfadhel, M. (author)
  • Molero-Luis, M. (author)
  • Darin, Niklas,1964Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics(Swepub:gu)xdarin (author)
  • Spiegel, R. (author)
  • de Coo, I. F. (author)
  • Gerards, M. (author)
  • Taylor, R. W. (author)
  • Artuch, R. (author)
  • Nashabat, M. (author)
  • Rodríguez-Pombo, P. (author)
  • Tabarki, B. (author)
  • Pérez-Dueñas, B. (author)
  • Distelmaier, F. (author)
  • Hahn, A. (author)
  • Morava, E. (author)
  • Banka, S. (author)
  • Debs, R. (author)
  • Fraser, J. L. (author)
  • Isohanni, P. (author)
  • Lähdesmäki, T. (author)
  • Livingston, J. (author)
  • Nadjar, Y. (author)
  • Schuler, E. (author)
  • Uusimaa, J. (author)
  • Vanderver, A. (author)
  • Friedman, J. R. (author)
  • Zimbric, M. R. (author)
  • McFarland, R. (author)
  • Santra, S. (author)
  • Wassmer, E. (author)
  • Martí-Sanchez, L. (author)
  • Darling, A. (author)
  • Göteborgs universitetInstitutionen för kliniska vetenskaper, Avdelningen för pediatrik (creator_code:org_t)

Related titles

  • In:Annals of Neurology: Wiley82:3, s. 317-3300364-5134

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