Literature DB >> 72134

Familial focal loss of cross striations.

G K van Wijngaarden, J Bethlem, K P Dingemans, C Coërs, N Telerman-Toppet, J M Gérard.   

Abstract

Two patients, a brother and sister, both suffering from congenital generalized muscle weakness with a progressive course are reported. Muscle biopsy revealed areas with loss of cross striations in the muscle fibers, electronmicroscopically presenting complete disorganization of the myofibrils with streaming of the Z discs and absence of mitochondria. Vesicular nuclei with prominent nucleoli were present in these areas. There was a type I fiber predominance in both cases. The mean diameter of the type I muscle fibers in one of the cases was too small. Motor endplate alterations in this patient gave no evidence of denervation but were suggestive of a delayed development of motor nerves.

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Year:  1977        PMID: 72134     DOI: 10.1007/BF00313617

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  13 in total

1.  [A case of amyotonia congenita characterized by a histological and histochemical anomalie of the neuromuscular junction].

Authors:  C COERS; S PELC
Journal:  Acta Neurol Psychiatr Belg       Date:  1954-02

2.  Terminal innervation ratio in neuromuscular disease. II. Disorders of lower motor neuron, peripheral nerve, and muscle.

Authors:  C Coërs; N Telerman-Toppet; J M Gerard
Journal:  Arch Neurol       Date:  1973-10

3.  Terminal innervation ratio in neuromuscular disease. I. Methods and controls.

Authors:  C Coërs; N Telerman-Toppet; J M Gérard
Journal:  Arch Neurol       Date:  1973-10

4.  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

5.  An electron microscopic study of target fibers, target-like fibers and related abnormalities in human muscle.

Authors:  D L Schotland
Journal:  J Neuropathol Exp Neurol       Date:  1969-04       Impact factor: 3.685

6.  Hypotrophic type I muscle fibres with central nuclei, and central myofibrillar lysis preferentially involving type II fibres.

Authors:  H Radu; V Ionescu; A Radu; V Paler; A M Roşu; A Marian
Journal:  Eur Neurol       Date:  1974       Impact factor: 1.710

Review 7.  Muscle biopsies in neuromuscular diseases.

Authors:  W K Engel
Journal:  Pediatr Clin North Am       Date:  1967-11       Impact factor: 3.278

8.  Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers.

Authors:  A G Engel; M R Gomez; R V Groover
Journal:  Mayo Clin Proc       Date:  1971-10       Impact factor: 7.616

9.  Congenital myopathy with target fibers.

Authors:  D L Schotland
Journal:  Trans Am Neurol Assoc       Date:  1967

10.  Neuromuscular disease with type I fiber atrophy, central nuclei, and myotube-like structures.

Authors:  J Bethlem; G K van Wijngaarden; A E Meijer; W C Hülsmann
Journal:  Neurology       Date:  1969-07       Impact factor: 9.910

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  4 in total

1.  Multicore myopathy associated with multiple pterygium syndrome and hypertrophic cardiomyopathy.

Authors:  M Ohkubo; T Ino; S Shimazaki; K Yabuto; R Okada; T Sato
Journal:  Pediatr Cardiol       Date:  1996 Jan-Feb       Impact factor: 1.655

2.  Autosomal dominant multicore disease.

Authors:  J A Vanneste; F C Stam
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-04       Impact factor: 10.154

3.  Pleocore disease. Multi-minicore disease and focal loss of cross striations.

Authors:  J J Martin; M Bruyland; H F Busch; J P Farriaux; I Krivosic; C Ceuterick
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

Review 4.  Multi-minicore Disease.

Authors:  Heinz Jungbluth
Journal:  Orphanet J Rare Dis       Date:  2007-07-13       Impact factor: 4.123

  4 in total

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