Literature DB >> 991722

Central core disease--a congenital myopathy.

J R Saper, H H Itabashi.   

Abstract

A case is reported of a 28-year-old woman with central core disease who prior to muscle biopsy was diagnosed to have muscular dystrophy. Histologic evaluation confirmed a diagnosis of central core disease, a nonprogressive or slowly progressive disorder of voluntary muscle belonging to a group of muscle diseases called benign congenital myopathies. The clinical and pathologic features fo this benign disorder are reviewed. Two sons were examined and found to be normal.

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Mesh:

Year:  1976        PMID: 991722

Source DB:  PubMed          Journal:  Dis Nerv Syst        ISSN: 0012-3714


  3 in total

1.  Central core disease in one of identical twins.

Authors:  M E Cohen; P K Duffner; R Heffner
Journal:  J Neurol Neurosurg Psychiatry       Date:  1978-07       Impact factor: 10.154

2.  Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter.

Authors:  L Palmucci; D Schiffer; G Monga; F Mollo; M de Marchi
Journal:  J Neurol       Date:  1978-04-14       Impact factor: 4.849

3.  Patterns of neuromuscular disease. As related to stages of normal embryogenesis in voluntary muscle.

Authors:  A Korényi-Both; G Marosán
Journal:  Am J Pathol       Date:  1979-05       Impact factor: 4.307

  3 in total

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