Literature DB >> 6213738

"Myopathic" changes in chorea-acanthocytosis. Clinical and histopathological studies.

L C Limos, A Ohnishi, T Sakai, N Fujii, I Goto, Y Kuroiwa.   

Abstract

Four cases of chorea-acanthocytosis were studied with special reference to muscular changes. All the cases showed the clinical stigmata of oro-linguo-facial dyskinesia with tongue biting, mild neurogenic muscular involvement and acanthocytosis. Serum creatine kinase (CK) was persistently elevated, showing MM type isozyme predominance. Histopathological studies of the peroneus brevis muscle showed prominent small group atrophy, increase of small fibers on diameter analysis, frequent angulated fibers, and angulated fibers with increased acid phosphatase activity. These findings are compatible with chronic denervation. However, central nucleation (approximately 10%) and fiber splitting (2-8%) were also found in all cases. These are compatible with myopathic changes. No correlation of these "myopathic" changes and serum CK levels was found. The "myopathic" findings are probably secondary to chronic denervation.

Entities:  

Mesh:

Substances:

Year:  1982        PMID: 6213738     DOI: 10.1016/0022-510x(82)90169-1

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


  5 in total

1.  Phenotypic Variation in a Caucasian Kindred with Chorea-Acanthocytosis.

Authors:  Áine Merwick; Tzehow Mok; Brian McNamara; Nollaig A Parfrey; Helena Moore; Brian J Sweeney; Collette K Hand; Aisling M Ryan
Journal:  Mov Disord Clin Pract       Date:  2014-12-06

2.  Amyotrophic choreo-acanthocytosis: a neuropathological and immunocytochemical study.

Authors:  S Galatioto; S Serra; D Batolo; T Marafioti
Journal:  Ital J Neurol Sci       Date:  1993-01

3.  Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus.

Authors:  A Malandrini; G M Fabrizi; S Palmeri; G Ciacci; C Salvadori; G Berti; A Bucalossi; A Federico; G C Guazzi
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

4.  Deficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic component.

Authors:  Elena Kudryashova; Jun Wu; Leif A Havton; Melissa J Spencer
Journal:  Hum Mol Genet       Date:  2009-01-19       Impact factor: 6.150

5.  Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement.

Authors:  Alessandro Vaisfeld; Giorgia Bruno; Martina Petracca; Anna Rita Bentivoglio; Serenella Servidei; Maria Gabriella Vita; Francesco Bove; Giulia Straccia; Clemente Dato; Giuseppe Di Iorio; Simone Sampaolo; Silvio Peluso; Anna De Rosa; Giuseppe De Michele; Melissa Barghigiani; Daniele Galatolo; Alessandra Tessa; Filippo Santorelli; Pietro Chiurazzi; Mariarosa Anna Beatrice Melone
Journal:  Genes (Basel)       Date:  2021-02-26       Impact factor: 4.096

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.