Literature DB >> 168319

A case of type 1 muscle fibre hypotrophy and internal nuclei.

T Inokuchi, H Umezaki, T Santa.   

Abstract

A 14 year old boy was diagnosed as suffering from type 1 muscle fibre hypotrophy with internal nuclei. On histological examination of a biopsied muscle, there was selective hypotrophy of type 1 muscle fibre with internal nuclei, and focal degenerative changes were seen in a few type 1 fibres. The small type 1 fibres were arranged in small or large groups in one bundle. An EMG study of moderately weak muscles revealed low amplitude and short duration motor unit potentials as well as normal potentials and no spontaneous discharges. The H reflexes were abnormally low in amplitude comapred with the M response. The histological and electrophysiological findings suggested that the type 1 fibre involvement in the present case may have a neurogenic basis. It is likely that the clinical features of the reported cases are too variable for a single clinical entity.

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Year:  1975        PMID: 168319      PMCID: PMC492000          DOI: 10.1136/jnnp.38.5.475

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  14 in total

1.  NEMALINE MYOPATHY; A SECOND CASE.

Authors:  W K ENGEL; T WANKO; G M FENICHEL
Journal:  Arch Neurol       Date:  1964-07

2.  A critique of the "myopathic" electromyogram.

Authors:  J R Warmolts; W K Engel
Journal:  Trans Am Neurol Assoc       Date:  1970

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Authors:  E Farkas-Bargeton; J Aicardi; J J Chevrie; S Thieffry
Journal:  Rev Neurol (Paris)       Date:  1968-12       Impact factor: 2.607

4.  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

5.  Histochemical studies of denervated or tenotomized cat muscle: illustrating difficulties in relating experimental animal conditions to human neuromuscular diseases.

Authors:  W K Engel; M H Brooke; P G Nelson
Journal:  Ann N Y Acad Sci       Date:  1966-09-09       Impact factor: 5.691

6.  Centronuclear myopathy in old age.

Authors:  D G Harriman; M A Haleem
Journal:  J Pathol       Date:  1972-11       Impact factor: 7.996

7.  Familial myopathy with probable lysis of myofibrils in type I fibers.

Authors:  P A Cancilla; K Kalyanaraman; M A Verity; T Munsat; C M Pearson
Journal:  Neurology       Date:  1971-06       Impact factor: 9.910

8.  Nemaline myopathy. I. Histochemical study.

Authors:  L Martin; J Reniers
Journal:  Acta Neuropathol       Date:  1968-11-01       Impact factor: 17.088

9.  Type I muscle fibre atrophy and central nuclei. A rare familial neuromuscular disease.

Authors:  G Karpati; S Carpenter; R F Nelson
Journal:  J Neurol Sci       Date:  1970-05       Impact factor: 3.181

10.  Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases.

Authors:  W K Engel
Journal:  Arch Neurol       Date:  1970-02
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  3 in total

1.  Congenital type II fibre deficient myopathy.

Authors:  J J Dinn; N O'Doherty
Journal:  Ir J Med Sci       Date:  1980-02       Impact factor: 1.568

2.  Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration.

Authors:  H Sugie; R Hanson; G Rasmussen; M A Verity
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-06       Impact factor: 10.154

3.  Myotonia in centronuclear myopathy.

Authors:  A Gil-Peralta; E Rafel; J Bautista; R Alberca
Journal:  J Neurol Neurosurg Psychiatry       Date:  1978-12       Impact factor: 10.154

  3 in total

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