Literature DB >> 1310292

Giant axonal neuropathy with predominant central nervous system manifestations.

Y Lampl1, Y Eshel, E Ben-David, R Gilad, I Sarova-Pinhas, U Sandbank.   

Abstract

The authors describe a 25-year-old woman with giant axonal neuropathy (GAN) and severe CNS involvement. She had been admitted to hospital with generalized seizures, and had gait disturbances followed by progressive mental deterioration since childhood. Neurological examination revealed mental retardation, scanning speech, cerebellar dysfunction, pyramidal signs, mainly in the lower extremities, and peripheral sensory neuropathy. Sensory nerve conduction velocity was decreased; brain CT and MRI showed diffuse demyelination. Sural nerve biopsy revealed characteristic signs of GAN. The patient's older sister had died at the age of 23, after having had similar neurological disturbances since childhood. This case illustrates an unfamiliar presentation of GAN, characterized by mild sensory neuropathy and serve CNS involvement, including seizures.

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Year:  1992        PMID: 1310292     DOI: 10.1111/j.1469-8749.1992.tb14983.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  2 in total

1.  Giant axonal neuropathy: clinical and genetic study in six cases.

Authors:  E Demir; P Bomont; S Erdem; L Cavalier; M Demirci; G Kose; S Muftuoglu; A N Cakar; E Tan; S Aysun; M Topcu; P Guicheney; M Koenig; H Topaloglu
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-06       Impact factor: 10.154

2.  3T MR with diffusion tensor imaging and single-voxel spectroscopy in giant axonal neuropathy.

Authors:  Christiana Brenner; Carlos Eduardo Speck-Martins; Luciano Farage; Peter B Barker
Journal:  J Magn Reson Imaging       Date:  2008-07       Impact factor: 4.813

  2 in total

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