Literature DB >> 6814164

A type of adult polyglucosan body disease.

K Okamoto, J F Llena, A Hirano.   

Abstract

Polyglucosan bodies in the nervous system and other viscera are the main findings at autopsy of a 64-year-old woman who had a chronic neurologic disorder of 20 years' duration. The clinical features included muscle weakness, sensory disturbances, neurogenic bladder, dementia, and cataracts. Light and electron microscopy of the nervous system showed numerous polyglucosan bodies in the processes of neurons and astrocytes but not in neuronal perikarya. A similar clinico-pathologic presentation has been described in six previous cases. It is suggested that this is a type of adult polyglucosan body disease which probably froms a variant of Lafora's disease.

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Year:  1982        PMID: 6814164     DOI: 10.1007/bf00692701

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  15 in total

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2.  Lafora's disease. An ultrastructural and histochemical study.

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Journal:  Acta Neuropathol       Date:  1974       Impact factor: 17.088

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Journal:  Arch Neurol       Date:  1971-07

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Authors:  H Jakob
Journal:  Acta Neuropathol       Date:  1969       Impact factor: 17.088

6.  Intraneuronal polyglucosan storage restricted to the lateral pallidum (Bielschowsky bodies). A golgi, light, and electron microscopic study.

Authors:  A Probst; P Sandoz; C Vanoni; J U Baumann
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

7.  A distinct form of adult polyglucosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes: a report of four cases and a review of the occurrence of polyglucosan bodies in other conditions such as Lafora's disease and normal ageing.

Authors:  Y Robitaille; S Carpenter; G Karpati; S D DiMauro
Journal:  Brain       Date:  1980-06       Impact factor: 13.501

8.  Adult polysaccharidosis. Clinicopathological, ultrastructural, and biochemical features.

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Journal:  Arch Neurol       Date:  1979-12

9.  Nervous system involvement in type IV glycogenosis.

Authors:  K R McMaster; J M Powers; G R Hennigar; H J Wohltmann; G H Farr
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10.  [On genetics of progressive myoclonic epilepsies (Unverricht-Lundborg)].

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Journal:  Humangenetik       Date:  1965
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  7 in total

1.  Intra-axonal polysaccharide deposits in the peripheral nerve seen in adult polysaccharide storage myopathy.

Authors:  O Komure; K Ichikawa; A Tsutsumi; K Hiyama; A Fujioka
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

2.  Polyglucosan bodies in sural nerve biopsies.

Authors:  H L Busard; A A Gabreëls-Festen; M A van 't Hof; W O Renier; F J Gabreëls
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

3.  Polyglucosan bodies in intramuscular motor nerves.

Authors:  R A Bernsen; H L Busard; H J Ter Laak; F J Gabreëls; W O Renier; E M Joosten; A G Theeuwes
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

4.  Sevoflurane anaesthesia for a patient with adult polyglucosan body disease.

Authors:  S Inoue; R Ishii; H Fukuda; K Saitoh; R Shimizu
Journal:  Can J Anaesth       Date:  1996-12       Impact factor: 5.063

5.  Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).

Authors:  J M Schröder; R May; Y S Shin; M Sigmund; S Nase-Hüppmeier
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

6.  Chronic demyelinating neuropathy and intra-axonal polyglucosan bodies.

Authors:  K Matsumuro; S Izumo; Y Minauchi; M Inose; I Higuchi; M Osame
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

7.  Dementia of frontal lobe type due to adult polyglucosan body disease.

Authors:  P Boulan-Predseil; A Vital; B Brochet; D Darriet; P Henry; C Vital
Journal:  J Neurol       Date:  1995-08       Impact factor: 4.849

  7 in total

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