Literature DB >> 6222163

Skeletal muscle in preterm infants with congenital myotonic dystrophy. Morphologic and histochemical study.

V Sahgal, S Bernes, S Sahgal, C Lischwey, V Subramani.   

Abstract

The skeletal muscle in 3 preterm infants (27, 34, 37 weeks gestation age) born to mothers with myotonic dystrophy showed a syncytial pattern at 27 weeks and a decreasing percentage of satellite cells and central nuclei at 34 and 37 weeks gestation. The fiber type differentiation was observed only at 37 weeks of gestational age. In all 3 cases muscle fibers with multiple acid phosphatase positive were seen. The muscle spindles also had thick capsules and showed lack of morphologic and histochemical differentiation into fiber types. These findings suggest immaturity of skeletal muscle in comparison to the normal. The immaturity of the skeletal muscle correlated well with the prognosis of the patients.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6222163     DOI: 10.1016/0022-510x(83)90080-1

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


  3 in total

1.  Ultrastructure of muscle spindle in congenital myotonic dystrophy. A study of preterm infant muscle spindles.

Authors:  V Sahgal; S Sahgal; S Bernes; V Subramani
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

2.  Benign congenital hypotonia with uniform type 1 fibers and aspecific ultrastructural changes in the muscle: a case with esophagus involvement.

Authors:  L G Spagnoli; G Palmieri; E Bertini
Journal:  Ital J Neurol Sci       Date:  1985-09

Review 3.  Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies.

Authors:  Guangbin Xia; Naohiro Terada; Tetsuo Ashizawa
Journal:  Curr Stem Cell Rep       Date:  2018-10-04
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.