Literature DB >> 7341555

Congenital fiber type disproportion with fatal outcome: a case report.

P Carboni, N Giacanelli, G Porro, G Sideri.   

Abstract

A child with congenital fiber type disproportion without structural changes in muscle fibres is reported. Although this pattern suggests a favorable prognosis, the clinical worsening followed by death at the age of 17 months shows that there is as yet no predictor for a benign course for this myopathy.

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Year:  1981        PMID： 7341555     DOI： 10.1007/bf02335415

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN： 0392-0461


  6 in total

1.  Type I fiber hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model.

Authors:  W K Engel; G N Gold; G Karpati
Journal:  Arch Neurol       Date:  1968-04

2.  Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook.

Authors:  N P Cavanagh; B D Lake; P McMeniman
Journal:  Arch Dis Child       Date:  1979-10       Impact factor: 3.791

3.  Muscle disorders in childhood.

Authors:  V Dubowitz
Journal:  Major Probl Clin Pediatr       Date:  1978

4.  [Neonatal hypotonias with congenital disproportion of various types of muscular fiber, especially type I fibers. Demonstration of the familial character of this new entity].

Authors:  M Fardeau; J P Harpey; B Caille; J Lafourcade
Journal:  Arch Fr Pediatr       Date:  1975-12

5.  The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies.

Authors:  M H Brooke; W K Engel
Journal:  Neurology       Date:  1969-06       Impact factor: 9.910

6.  Clinical variability in congenital fiber type disproportion.

Authors:  R R Clancy; K A Kelts; J W Oehlert
Journal:  J Neurol Sci       Date:  1980-06       Impact factor: 3.181
  6 in total

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