Literature DB >> 6934069

Muscle phosphorylase deficiency in childhood.

R C Sengers, A M Stadhouders, H H Jaspar, K J Lamers, J M Trijbels, S L Notermans.   

Abstract

Myophosphorylase deficiency (McArdle's syndrome) is an uncommon condition characterized by exercise intolerance, muscle cramps and myoglobinuria. The present report describes the clinical, histochemical, electronmicroscopic and biochemical findings in a 12-year-old boy with myophosphorylase deficiency. The diagnosis should have been suspected when the boy was 6 years old. Most index cases have not been diagnosed until adult life, but this syndrome has to be considered in the differential diagnosis of exercise intolerance in childhood.

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Year:  1980        PMID: 6934069     DOI: 10.1007/bf01846039

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  11 in total

1.  Fatal infantile form of muscle phosphorylase deficiency.

Authors:  S DiMauro; P L Hartlage
Journal:  Neurology       Date:  1978-11       Impact factor: 9.910

2.  Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle.

Authors:  R SCHMID; R MAHLER
Journal:  J Clin Invest       Date:  1959-11       Impact factor: 14.808

3.  Myopathy due to a defect in muscle glycogen breakdown.

Authors:  B McARDLE
Journal:  Clin Sci       Date:  1951-02       Impact factor: 6.124

4.  GLYCOGEN SYNTHESIS IN MUSCLE LACKING PHOSPHORYLASE.

Authors:  R Schmid; P W Robbins; R R Traut
Journal:  Proc Natl Acad Sci U S A       Date:  1959-08       Impact factor: 11.205

5.  A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE.

Authors:  W F Mommaerts; B Illingworth; C M Pearson; R J Guillory; K Seraydarian
Journal:  Proc Natl Acad Sci U S A       Date:  1959-06       Impact factor: 11.205

6.  Comparison of two methods for the assay of glycogen phosphorylase in tissue homogenates.

Authors:  V A Mezl; W E Knox
Journal:  Enzyme       Date:  1972

7.  [McArdle's disease--description based on three own observations (author's transl)].

Authors:  M Berger; E Gibbels; B Leven; D Seiler
Journal:  Fortschr Neurol Psychiatr Grenzgeb       Date:  1978-06

8.  [McArdle's syndrome (myopathy in muscle phosphorylase deficiency)].

Authors:  K Schimrigk; H G Mertens; K Ricker; J Führ; P Eyer; D Pette
Journal:  Klin Wochenschr       Date:  1967-01-01

9.  Myophosphorylase deficiency: two different molecular etiologies.

Authors:  H Feit; M H Brooke
Journal:  Neurology       Date:  1976-10       Impact factor: 9.910

10.  Lactate production in McArdle's disease.

Authors:  A K Baksi; P H Buxton; P Cochrane; R R Hughes
Journal:  Postgrad Med J       Date:  1977-03       Impact factor: 2.401

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  2 in total

1.  Fetal congenital lethal hypophosphatasia: histochemical absence of alkaline phosphatase activity in endothelial cells of intramuscular capillaries.

Authors:  H H Goebel; M Schlie; U Burck
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

Review 2.  Muscle fatigue during high-intensity exercise in children.

Authors:  Sébastien Ratel; Pascale Duché; Craig A Williams
Journal:  Sports Med       Date:  2006       Impact factor: 11.928

  2 in total

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