Literature DB >> 8352860

Myopathy with abnormal distribution of dystrophin, growth retardation, mental retardation, and hypospadia.

T Nagai1, Y Tuchiya, A Maruyama, R Sakuta, I Nonaka.   

Abstract

A 9-year-old boy with severe growth retardation, mild mental retardation, and hypospadia had a high serum CK level without muscle weakness and atrophy. Muscle biopsy revealed a moderate variation in fiber size with a few necrotic and scattered regenerating fibers. Although muscle membranes were clearly stained by immunostaining with antibody to dystrophin, N-terminal region (2-5E2), fibers in groups revealed striking, intense staining with the other antibody, C-terminal region (4C5), suggesting some aberration of the dystrophin gene near the C-terminal area. His unique clinical features, as well as myopathy, are reported, although further study is necessary to clarify the relationship between the anomalous conditions and dystrophin abnormalities.

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Year:  1993        PMID: 8352860     DOI: 10.1016/0887-8994(93)90094-s

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  2 in total

1.  Influence of dystrophin-gene mutation on mdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks.

Authors:  C Vaillend; A Rendon; R Misslin; A Ungerer
Journal:  Behav Genet       Date:  1995-11       Impact factor: 2.805

2.  Severe dystrophinopathy in a patient with congenital hypotonia.

Authors:  G Cordone; M Bado; G Morreale; M Pedemonte; C Minetti
Journal:  Childs Nerv Syst       Date:  1996-08       Impact factor: 1.475

  2 in total

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