Literature DB >> 9638664

Marinesco Sjögren syndrome with rhabdomyolysis. A new subtype of the disease.

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.

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Year:  1998        PMID: 9638664     DOI: 10.1055/s-2007-973542

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  3 in total

Review 1.  MR imaging features in Marinesco-Sjögren syndrome: severe cerebellar atrophy is not an obligatory finding.

Authors:  Anke Reinhold; Ianina Scheer; Rüdiger Lehmann; Luitgard M Neumann; Theodor Michael; Raymonda Varon; Arpad Von Moers
Journal:  AJNR Am J Neuroradiol       Date:  2003-05       Impact factor: 3.825

2.  MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline elevated  serum creatine kinase.

Authors:  Osorio Lopes Abath Neto; Livija Medne; Sandra Donkervoort; Maria Elena Rodríguez-García; Véronique Bolduc; Ying Hu; Eleonora Guadagnin; A Reghan Foley; John F Brandsema; Allan M Glanzman; Gihan I Tennekoon; Mariarita Santi; Justin H Berger; Lynn A Megeney; Hirofumi Komaki; Michio Inoue; Francisco Javier Cotrina-Vinagre; Aurelio Hernández-Lain; Elena Martin-Hernández; Linford Williams; Sabine Borell; David Schorling; Kimberly Lin; Konstantinos Kolokotronis; Uta Lichter-Konecki; Janbernd Kirschner; Ichizo Nishino; Brenda Banwell; Francisco Martínez-Azorín; Patrick G Burgon; Carsten G Bönnemann
Journal:  Brain       Date:  2021-10-22       Impact factor: 15.255

Review 3.  Rhabdomyolysis: a genetic perspective.

Authors:  Renata Siciliani Scalco; Alice R Gardiner; Robert Ds Pitceathly; Edmar Zanoteli; Jefferson Becker; Janice L Holton; Henry Houlden; Heinz Jungbluth; Ros Quinlivan
Journal:  Orphanet J Rare Dis       Date:  2015-05-02       Impact factor: 4.123

  3 in total

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