| Literature DB >> 9638664 |
W Müller-Felber1, D Zafiriou, R Scheck, I Pätzke, M Toepfer, D E Pongratz, U Walther.
Abstract
Four children from two families with characteristics of Marinesco-Sjögren syndrome (congenital cataract, ataxia) are presented. All children had clinical and neurophysiological signs of a demyelinating polyneuropathy. Three of them developed acute rhabdomyolysis with marked weakness and CK levels of up to 40,000 U/I following a viral infection. In all children CK levels returned to normal within two weeks. Symptoms were recurrent in one of the children and resulted in a severe disability. In two other children recovery of motor function took about a month following the first attack. Metabolic disorders of the muscle were excluded by pathobiochemical examination of a muscle biopsy in one of the children. In conclusion, acute rhabdomyolysis can occur as a neuromuscular complication of Marinesco-Sjögren syndrome.Entities:
Mesh:
Year: 1998 PMID: 9638664 DOI: 10.1055/s-2007-973542
Source DB: PubMed Journal: Neuropediatrics ISSN: 0174-304X Impact factor: 1.947