Literature DB >> 6830453

Nonprogressive congenital neuromuscular disease with uniform type 1 fiber.

S J Oh, M J Danon.   

Abstract

Three patients had nonprogressive congenital neuromuscular disease with uniform type 1 fiber. Uniform fiber type was defined as more than 99% of muscle fibers belonging to one type. These cases were characterized by early onset of symptoms, mild proximal weakness, hyporeflexia or areflexia, normal serum muscle enzyme levels, short duration of motor unit potentials, uniform type 1 fibers, and nonprogression. These cases represent a distinct form of nonprogressive congenital neuromuscular disease.

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Year:  1983        PMID: 6830453     DOI: 10.1001/archneur.1983.04050030041007

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  3 in total

1.  Comparison of clinical characteristics between congenital fiber type disproportion myopathy and congenital myopathy with type 1 fiber predominance.

Authors:  Sang-Jun Na; Woo-Kyung Kim; Tai-Seung Kim; Seong-Woong Kang; Eun-Young Lee; Young-Chul Choi
Journal:  Yonsei Med J       Date:  2006-08-31       Impact factor: 2.759

2.  Kyphoscoliosis associated with congenital neuromuscular disease with uniform type 1 fibers.

Authors:  Shiro Imagama; Noriaki Kawakami; Taichi Tsuji; Tetsuya Ohara; Naoki Ishiguro
Journal:  Eur Spine J       Date:  2011-12-23       Impact factor: 3.134

3.  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
  3 in total

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