Literature DB >> 2522540

Muscle pathology in Marinesco-Sjögren syndrome.

A Komiyama1, I Nonaka, K Hirayama.   

Abstract

Three of 4 adult patients with Marinesco-Sjögren syndrome (MSS; 2 males and 2 females, aged 26-31 years) in 2 families became non-ambulant because of slowly progressive muscular weakness rather than cerebellar ataxia. Other clinical features in these 4 patients were typical for MSS: bilateral cataracts from infancy, mental retardation, severe cerebellar atrophy, multiple skeletal abnormalities and hypergonadotropic hypogonadism. EMG demonstrated a myopathic pattern and serum CK was mildly elevated. Muscle biopsies from these 3 patients showed myopathic changes including a marked variation in fiber size, an increased number of fibers with centralized nuclei, and scattered necrotic and regenerating fibers. Fiber type analysis with myosin ATPase staining showed type 1 fiber predominance, type 2B fiber deficiency and mild increase in type 2C fibers. Muscle biopsy changes and the clinical course indicate that our MSS patients suffered from a chronic dystrophic process similar to that in congenital muscular dystrophy.

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Year:  1989        PMID: 2522540     DOI: 10.1016/0022-510x(89)90010-5

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  6 in total

1.  Myopathy is a prominent feature in Marinesco-Sjögren syndrome: A muscle computed tomography study.

Authors:  Ibrahim Mahjneh; Anna-Kaisa Anttonen; Mirja Somer; Anders Paetau; Anna-Elina Lehesjoki; Hannu Somer; Bjarne Udd
Journal:  J Neurol       Date:  2005-09-15       Impact factor: 4.849

2.  Myopathy in Marinesco-Sjögren syndrome: an ultrastructural study.

Authors:  Y Goto; A Komiyama; Y Tanabe; Y Katafuchi; E Ohtaki; I Nonaka
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

Review 3.  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

4.  Congenital muscular dystrophy and severe central nervous system atrophy in two siblings.

Authors:  Q H Leyten; P G Barth; F J Gabreëls; K Renkawek; W O Renier; A A Gabreëls-Festen; H J ter Laak; M G Smits
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

5.  Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

Authors:  Wahiba Hamza; Lamia Ali Pacha; Tarik Hamadouche; Jean Muller; Nathalie Drouot; Farida Ferrat; Samira Makri; Malika Chaouch; Meriem Tazir; Michel Koenig; Traki Benhassine
Journal:  BMC Med Genet       Date:  2015-06-12       Impact factor: 2.103

Review 6.  Role of the HSP70 Co-Chaperone SIL1 in Health and Disease.

Authors:  Viraj P Ichhaporia; Linda M Hendershot
Journal:  Int J Mol Sci       Date:  2021-02-04       Impact factor: 5.923

  6 in total

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