Literature DB >> 284761

Nervous system involvement in type IV glycogenosis.

K R McMaster, J M Powers, G R Hennigar, H J Wohltmann, G H Farr.   

Abstract

A 30-month-old girl exhibited the 19th known case of type IV glycogenosis. Extensive involvement of the nervous system was found at autopsy. This represents only the second patient in whom the fine structure of the CNS and skeletal muscle has been described. We have also identified the abnormal polysaccharide in peripheral nerve, a finding that, to our knowledge, has not been reported previously. Our review of the literature indicates that approximately 50% of these patients exhibit signs or symptoms referable to the neuromuscular system. Most clinical and pathologic studies have focused on the severe liver involvement; insufficient attention has been directed toward the nervous system. This emphasizes the need for more detailed neurologic and neuropathologic examinations of children with type IV glycogenosis.

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Year:  1979        PMID: 284761

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  19 in total

1.  [Polyglycosan body myopathy].

Authors:  M Jeub; K Kappes-Horn; C Kornblum; D Fischer
Journal:  Nervenarzt       Date:  2006-12       Impact factor: 1.214

2.  Liver transplantation for type IV glycogen storage disease.

Authors:  R Selby; T E Starzl; E Yunis; B I Brown; R S Kendall; A Tzakis
Journal:  N Engl J Med       Date:  1991-01-03       Impact factor: 91.245

3.  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

4.  Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes.

Authors:  Y S Shin; H Steigüber; P Klemm; W Endres; O Schwab; G Wolff
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

Review 5.  Cell migration and chimerism after whole-organ transplantation: the basis of graft acceptance.

Authors:  T E Starzl; A J Demetris; M Trucco; N Murase; C Ricordi; S Ildstad; H Ramos; S Todo; A Tzakis; J J Fung
Journal:  Hepatology       Date:  1993-06       Impact factor: 17.425

Review 6.  Glycogen storage diseases in animals and their potential value as models of human disease.

Authors:  H C Walvoort
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

7.  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

8.  Dicarboxylicaciduria and secondary carnitine deficiency in glycogenosis type IV.

Authors:  P D Maaswinkel-Mooy; B J Poorthuis; H H van Gelderen; J J van de Kamp
Journal:  Arch Dis Child       Date:  1987-10       Impact factor: 3.791

9.  Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis.

Authors:  T T Tang; A D Segura; Y T Chen; L M Ricci; R A Franciosi; M L Splaingard; M S Lubinsky
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

10.  Liver transplantation for type I and type IV glycogen storage disease.

Authors:  R Selby; T E Starzl; E Yunis; S Todo; A G Tzakis; B I Brown; R S Kendall
Journal:  Eur J Pediatr       Date:  1993       Impact factor: 3.183

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