Literature DB >> 23689405

Muscle biopsy in Pompe disease.

Lineu Cesar Werneck1, Paulo José Lorenzoni, Cláudia Suemi Kamoi Kay, Rosana Herminia Scola.   

Abstract

UNLABELLED: Pompe disease (PD) can be diagnosed by measuring alpha-glucosidase levels or by identifying mutations in the gene enzyme. Muscle biopsies can aid diagnosis in doubtful cases.
METHODS: A review of muscle biopsy from 19 cases of PD (infantile, 6 cases; childhood, 4 cases; and juvenile/adult, 9 cases).
RESULTS: Vacuoles with or without glycogen storage were found in 18 cases. All cases had increased acid phosphatase activity. The vacuole frequency varied (almost all fibers in the infantile form to only a few in the juvenile/adult form). Atrophy of type 1 and 2 fibers was frequent in all forms. Atrophic angular fibers in the NADH-tetrazolium reductase and nonspecific esterase activity were observed in 4/9 of the juvenile/adult cases.
CONCLUSION: Increased acid phosphatase activity and vacuoles were the primary findings. Most vacuoles were filled with glycogen, and the adult form of the disease had fewer fibers with vacuoles than the infantile or childhood forms.

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Mesh:

Year:  2013        PMID: 23689405     DOI: 10.1590/0004-282x20130022

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  6 in total

1.  Micropatterned substrates with physiological stiffness promote cell maturation and Pompe disease phenotype in human induced pluripotent stem cell-derived skeletal myocytes.

Authors:  Nunnapas Jiwlawat; Eileen M Lynch; Brett N Napiwocki; Alana Stempien; Randolph S Ashton; Timothy J Kamp; Wendy C Crone; Masatoshi Suzuki
Journal:  Biotechnol Bioeng       Date:  2019-06-20       Impact factor: 4.530

Review 2.  Pompe disease: literature review and case series.

Authors:  Majed Dasouki; Omar Jawdat; Osama Almadhoun; Mamatha Pasnoor; April L McVey; Ahmad Abuzinadah; Laura Herbelin; Richard J Barohn; Mazen M Dimachkie
Journal:  Neurol Clin       Date:  2014-08       Impact factor: 3.806

3.  The infantile-onset form of Pompe disease: an autopsy diagnosis.

Authors:  Otávio César Cruz Dos Santos; Regina Schultz
Journal:  Autops Case Rep       Date:  2015-12-30

4.  Satellite cells fail to contribute to muscle repair but are functional in Pompe disease (glycogenosis type II).

Authors:  Lydie Lagalice; Julien Pichon; Eliot Gougeon; Salwa Soussi; Johan Deniaud; Mireille Ledevin; Virginie Maurier; Isabelle Leroux; Sylvie Durand; Carine Ciron; Francesca Franzoso; Laurence Dubreil; Thibaut Larcher; Karl Rouger; Marie-Anne Colle
Journal:  Acta Neuropathol Commun       Date:  2018-10-31       Impact factor: 7.801

5.  Interleukin-1 Beta and Tumor Necrosis Factor Alpha Upregulation and Nuclear Factor Kappa B Activation in Skeletal Muscle from a Mouse Model of Chronic/Progressive Parkinson Disease.

Authors:  Nour Erekat; Muhammed D Al-Jarrah
Journal:  Med Sci Monit       Date:  2018-10-22

6.  Clinical and molecular characterization of Korean children with infantile and late-onset Pompe disease: 10 years of experience with enzyme replacement therapy at a single center.

Authors:  Min-Sun Kim; Ari Song; Minji Im; June Huh; I-Seok Kang; Jinyoung Song; Aram Yang; Jinsup Kim; Eun-Kyung Kwon; Eu-Jin Choi; Sun-Ju Han; Hyung-Doo Park; Sung Yoon Cho; Dong-Kyu Jin
Journal:  Korean J Pediatr       Date:  2018-10-04
  6 in total

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