| Literature DB >> 1407389 |
P Uvebrant1, K Lanneskog, B Hagberg.
Abstract
Progressive encephalopathies in the west Swedish region were investigated in a population-based study. Cases were allocated to one of five main groups: 1) disorders covered by impairments in subcellular organelles, 2) disorders covered by deficiencies in the intermediate metabolism, 3) biochemically undefined neurometabolic disorders, 4) neuroimmunological disorders and 5) a symptom-orientated miscellaneous group. Progressive encephalopathies were identified in 76 of 132,138 children born alive in the study area during the 16-year-period 1970-85. This gives a live birth prevalence of 0.58 per 1000. In Sweden the size of the group corresponds to that of neural tube defects and that of congenital hydrocephalus. However, a vast number of different disorders are represented.Entities:
Mesh:
Year: 1992 PMID: 1407389 DOI: 10.1055/s-2008-1071343
Source DB: PubMed Journal: Neuropediatrics ISSN: 0174-304X Impact factor: 1.947