Literature DB >> 2793417

Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype.

M Mondelli1, A Rossi, S Palmeri, N Rizzuto, A Federico.   

Abstract

We report the electrophysiological investigation of two adult cases with GM 2 gangliosidosis with hexosaminidase A and B deficiency. Superficial peroneal biopsy was obtained from one patient. The electrophysiological alterations of the peripheral nervous system were fasciculations, signs of collateral reinnervation and loss of motor units, decrease in sensory potential amplitude and increase in distal motor latency. Increase in N9-N13 interpeak latency of the somatosensory evoked potentials and an increase I-V interpeak latency of the brain-stem auditory potentials were evident in both cases. Visual evoked potentials were normal. Nerve biopsy showed a severe loss of myelinated fibers, especially of those with the largest diameter, with no signs of segmental demyelination, or remyelination. A tentative interpretation of our findings is given.

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Year:  1989        PMID: 2793417     DOI: 10.1007/bf02334949

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  25 in total

1.  Adult (chronic) GM2 gangliosidosis. Atypical spinocerebellar degeneration in a Jewish sibship.

Authors:  I Rapin; K Suzuki; K Suzuki; M P Valsamis
Journal:  Arch Neurol       Date:  1976-02

2.  N-acetyl-beta-hexosaminidase B deficiency in cultured fibroblasts from a patient with progressive motor neuron disease.

Authors:  L W Hancock; A L Horwitz; N R Cashman; J P Antel; G Dawson
Journal:  Biochem Biophys Res Commun       Date:  1985-08-15       Impact factor: 3.575

3.  Auditory dysfunction in Friedreich ataxia: result of spiral ganglion degeneration.

Authors:  S Satya-Murti; A Cacace; P Hanson
Journal:  Neurology       Date:  1980-10       Impact factor: 9.910

4.  Central distal axonopathy syndromes: newly recognized models of naturally occurring human degenerative disease.

Authors:  P K Thomas; H H Schaumburg; P S Spencer; H E Kaeser; C A Pallis; F C Rose; N H Wadia
Journal:  Ann Neurol       Date:  1984-04       Impact factor: 10.422

5.  Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotype.

Authors:  W G Johnson; H J Wigger; H R Karp; L M Glaubiger; L P Rowland
Journal:  Ann Neurol       Date:  1982-01       Impact factor: 10.422

6.  Spinocerebellar degeneration: hexosaminidase A and B deficiency in two adult sisters.

Authors:  J G Oonk; H J van der Helm; J J Martin
Journal:  Neurology       Date:  1979-03       Impact factor: 9.910

7.  Juvenile progressive dystonia: a new phenotype of GM2 gangliosidosis.

Authors:  D Meek; L S Wolfe; E Andermann; F Andermann
Journal:  Ann Neurol       Date:  1984-04       Impact factor: 10.422

8.  Hexosaminidase A deficiency in adults.

Authors:  R Navon; Z Argov; A Frisch
Journal:  Am J Med Genet       Date:  1986-05

9.  A new juvenile hexosaminidase deficiency disease presenting as cerebellar ataxia. Clinical and biochemical studies.

Authors:  W G Johnson; A Chutorian; A Miranda
Journal:  Neurology       Date:  1977-11       Impact factor: 9.910

10.  Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: clinical, morphologic, and biochemical studies of nine cases.

Authors:  J P Willner; G A Grabowski; R E Gordon; A N Bender; R J Desnick
Journal:  Neurology       Date:  1981-07       Impact factor: 9.910

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  6 in total

1.  Peripheral and autonomic nervous system involvement in chronic GM2-gangliosidosis.

Authors:  M S Salman; J T Clarke; G Midroni; M B Waxman
Journal:  J Inherit Metab Dis       Date:  2001-02       Impact factor: 4.982

2.  Achalasia in a patient with adult-onset Tay-Sachs disease.

Authors:  Jeffrey W Nathanson; Charles S Winans
Journal:  Dig Dis Sci       Date:  2006-01       Impact factor: 3.199

Review 3.  Lysosomal storage diseases.

Authors:  Carlos R Ferreira; William A Gahl
Journal:  Transl Sci Rare Dis       Date:  2017-05-25

4.  Early and severe sensory loss in three adult siblings with hexosaminidase A and B deficiency (Sandhoff disease).

Authors:  H Schnorf; R Gitzelmann; N U Bosshard; M Spycher; W Waespe
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-11       Impact factor: 10.154

5.  Repetitive long-term hyperbaric oxygen treatment (HBOT) administered after experimental traumatic brain injury in rats induces significant remyelination and a recovery of sensorimotor function.

Authors:  Klaus Kraitsy; Muammer Uecal; Stefan Grossauer; Lukas Bruckmann; Florentina Pfleger; Stefan Ropele; Franz Fazekas; Gerda Gruenbacher; Silke Patz; Markus Absenger; Christian Porubsky; Freyja Smolle-Juettner; Irem Tezer; Marek Molcanyi; Ulrike Fasching; Ute Schaefer
Journal:  PLoS One       Date:  2014-05-21       Impact factor: 3.240

6.  Peripheral nervous system manifestations in a Sandhoff disease mouse model: nerve conduction, myelin structure, lipid analysis.

Authors:  Melanie A McNally; Rena C Baek; Robin L Avila; Thomas N Seyfried; Gary R Strichartz; Daniel A Kirschner
Journal:  J Negat Results Biomed       Date:  2007-07-10
  6 in total

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