Literature DB >> 21321956

Clinical and pathological features in 15 Chinese patients with calpainopathy.

Su-Shan Luo1, Jian-Ying Xi, Jia-Hong Lu, Chong-Bo Zhao, Wen-Hua Zhu, Jie Lin, Yin Wang, Hui-Min Ren, Bo Yin, Urtizberea J Andoni.   

Abstract

BACKGROUND: Calpainopathy is comprised of a group of myopathies caused by deficiency in calcium-activated, neutral protease (calpain-3). In this study we identify calpainopathy in a cohort of Chinese patients with unclassified myopathy and analyze its clinical and pathological features.
METHODS: Sixty-six muscle biopsies were selected for combined Western blotting of dysferlin and calpain-3 after immunohistochemical staining. Clinical and pathological parameters of 15 confirmed calpainopathy cases were determined.
RESULTS: The diagnosis of calpainopathy in 15 Chinese patients was confirmed by Western blot analysis. Fourteen subjects had progressive proximal muscle weakness; 1 presented with bilateral distal muscle atrophy of the lower extremities. Scapular winging was observed in 12 patients (80%), and joint contractures were found in 10 others (66.7%). Histopathological studies showed a high prevalence of lobulated fibers (66.7%).
CONCLUSIONS: Chinese patients with calpainopathy share some common clinical and pathological features with the reported characteristics of non-Chinese patients.
Copyright © 2010 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 21321956     DOI: 10.1002/mus.21908

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  4 in total

1.  Natural history of LGMD2A for delineating outcome measures in clinical trials.

Authors:  Isabelle Richard; Jean-Yves Hogrel; Daniel Stockholm; Christine A M Payan; Françoise Fougerousse; Bruno Eymard; Claude Mignard; Adolfo Lopez de Munain; Michel Fardeau; Jon Andoni Urtizberea
Journal:  Ann Clin Transl Neurol       Date:  2016-03-04       Impact factor: 4.511

2.  Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing.

Authors:  Meng Yu; Yiming Zheng; Suqin Jin; Qiang Gang; Qingqing Wang; Peng Yu; He Lv; Wei Zhang; Yun Yuan; Zhaoxia Wang
Journal:  PLoS One       Date:  2017-04-12       Impact factor: 3.240

3.  NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay.

Authors:  Fabiola Mavillard; Marcos Madruga-Garrido; Eloy Rivas; Emilia Servián-Morilla; Rainiero Ávila-Polo; Irene Marcos; Francisco J Morón; Carmen Paradas; Macarena Cabrera-Serrano
Journal:  Ann Clin Transl Neurol       Date:  2019-10-14       Impact factor: 4.511

4.  Limb-girdle muscular dystrophy subtypes: First-reported cohort from northeastern China.

Authors:  Omar Abdulmonem Mahmood; Xinmei Jiang; Qi Zhang
Journal:  Neural Regen Res       Date:  2013-07-15       Impact factor: 5.135

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.