Literature DB >> 3701365

Clinical-anatomic study of a family with bulbo-spinal muscular atrophy in adults.

D Schiffer, F Brignolio, A Chio, M T Giordana, A Migheli.   

Abstract

Four cases are presented, with bulbo-spinal muscular atrophy characterised by adult onset and rapid evolution. They belong to a family in which the type of inheritance is probably dominant. Two cases were studied histologically. The most striking feature was the disappearance of neurons in the lower motor nuclei of medulla and of the spinal anterior horns. An electron microscopic study was carried out in one case. Accumulation of neurofilaments was a general characteristic, in addition to the picture of different sized spheroids. The clinical-pathological relationship is discussed.

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Year:  1986        PMID: 3701365     DOI: 10.1016/0022-510x(86)90058-4

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  3 in total

1.  Kennedy's disease: clinical and molecular study of two Italian families.

Authors:  D Pareyson; B Castellotti; S Botti; C A Defanti; C Gellera; F Taroni; A Sghirlanzoni
Journal:  Ital J Neurol Sci       Date:  1995-10

2.  Familial bulbospinal neuronopathy with optic atrophy: a distinct entity.

Authors:  G Paradiso; F Micheli; A L Taratuto; I C Parera
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-08       Impact factor: 10.154

3.  Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-van Laere syndrome or Madras-type motor neuron disease?

Authors:  B A Summers; M Swash; M S Schwartz; D A Ingram
Journal:  J Neurol       Date:  1987-08       Impact factor: 4.849

  3 in total

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