Literature DB >> 567119

Recurrent exertional rhabdomyolysis and stunted growth.

R C Sengers, A M Stadhouders, J M Trijbels, H H Jaspar.   

Abstract

A boy with recurrent exertional rhabdomyolysis and stunted growth is described. Fetal movements were few and the boy was small for gestational age. He always experienced easy fatigability, and he noted bouts of pigmenturia associated with episodes of considerable malaise. The change in color of the urine was caused by myoglobin. An electromyogram was myopathic. CPK rose during 60 minutes mild exercise. Prolonged moderate exercise could not be performed. Histopathological examination of muscle biopsy revealed an increase in the number of 11C fibres (20%). Electronmicroscopy revealed the wavy outline of a number of fibres and hypertrophy of sarcoplasmic reticulum elements. No cause for the stunted growth could be detected.

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Year:  1978        PMID: 567119     DOI: 10.1007/bf00442373

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


  18 in total

1.  The clinical syndrome of paroxysmal paralytic myoglobinuria. Report of 2 cases and an analytical review of the literature.

Authors:  J KOREIN; D R CODDON; F H MOWREY
Journal:  Neurology       Date:  1959-11       Impact factor: 9.910

2.  Mitochondrial myopathy with multisystem abnormalities and normal ocular movements.

Authors:  J G McLeod; W de C Baker; C D Shorey; C B Kerr
Journal:  J Neurol Sci       Date:  1975-01       Impact factor: 3.181

3.  Exercise myoglobinemia and acute exertional rhabdomyolysis.

Authors:  M A Demos; E L Gitin; L J Kagen
Journal:  Arch Intern Med       Date:  1974-10

4.  Chronic lactic acidosis in association with myopathy.

Authors:  M J Terlow; B D Lake; J K Lloyd
Journal:  Arch Dis Child       Date:  1973-06       Impact factor: 3.791

5.  A method for the determination of carnitine in the picomole range.

Authors:  G Cederblad; S Lindstedt
Journal:  Clin Chim Acta       Date:  1972-03       Impact factor: 3.786

6.  A skeletal-muscle disorder associated with intermittent symptoms and a possible defect of lipid metabolism.

Authors:  W K Engel; N A Vick; C J Glueck; R I Levy
Journal:  N Engl J Med       Date:  1970-03-26       Impact factor: 91.245

7.  The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiologic features.

Authors:  G Karpati; S Carpenter; A G Engel; G Watters; J Allen; S Rothman; G Klassen; O A Mamer
Journal:  Neurology       Date:  1975-01       Impact factor: 9.910

8.  Skeletal muscle disease with abnormal mitochondria.

Authors:  G K van Wijngaarden; J Bethlem; A E Meijer; W C Hülsmann; C A Feltkamp
Journal:  Brain       Date:  1967-09       Impact factor: 13.501

9.  Carnitine-palmityl-transferase deficiency.

Authors:  W J Cumming; M Hardy; P Hudgson; J Walls
Journal:  J Neurol Sci       Date:  1976-12       Impact factor: 3.181

10.  Cardiomyopathy and short stature associated with mitochondrial and/or lipid storage myopathy of skeletal muscle.

Authors:  R C Sengers; A M Stadhouders; H H Jaspar; J M Trijbels; O Daniels
Journal:  Neuropadiatrie       Date:  1976-05
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