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. 1964 Oct;27(5):361–380. doi: 10.1136/jnnp.27.5.361

Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis1

L -E Larsson 1,2, H Linderholm 1,2, R Müller 1,2, T Ringqvist 1,2, R Sörnäs 1,2
PMCID: PMC495765  PMID: 14213465

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ACHESON D., McALPINE D. Muscular dystrophy associated with paroxysmal myoglobinuria and excessive excretion of ketosteroids. Lancet. 1953 Aug 22;265(6782):372–375. doi: 10.1016/s0140-6736(53)91404-4. [DOI] [PubMed] [Google Scholar]
  2. AZZONE G. F., EEG-OLOFSSON O., ERNSTER L., LUFT R., SZABOLCSI G. Studies on isolated human skeletal muscle mitochondria. Exp Cell Res. 1961 Jan;22:415–436. doi: 10.1016/0014-4827(61)90119-7. [DOI] [PubMed] [Google Scholar]
  3. BERENBAUM M. C., BIRCH C. A., MORELAND J. D. Paroxysmal myoglobinuria. Lancet. 1955 Apr 30;268(6870):892–896. doi: 10.1016/s0140-6736(55)90380-9. [DOI] [PubMed] [Google Scholar]
  4. BOWDEN D. H., FRASER D., JACKSON S. H., WALKER N. F. Acute recurrent rhabdomyolysis (paroxysmal myohaemoglobinuria); a report of three cases and a review of the literature. Medicine (Baltimore) 1956 Dec;35(4):335–353. [PubMed] [Google Scholar]
  5. BUCHTHAL F., GULD C., ROSENFALCK P. Action potential parameters in normal human muscle and their dependence on physical variables. Acta Physiol Scand. 1954 Nov;32(2-3):200–218. doi: 10.1111/j.1748-1716.1954.tb01167.x. [DOI] [PubMed] [Google Scholar]
  6. CARLSON L. A., PERNOW B. Oxygen utilization and lactic acid formation in the legs at rest and during exercise in normal subjects and in patients with arteriosclerosis obliterans. Acta Med Scand. 1959 May 20;164(1):39–52. doi: 10.1111/j.0954-6820.1959.tb00163.x. [DOI] [PubMed] [Google Scholar]
  7. DAUGHERTY G. W., KAYE R. L., MATHIESON D. R. Idiopathic paroxysmal myoglobinuria. Proc Staff Meet Mayo Clin. 1959 Aug 5;34:395–397. [PubMed] [Google Scholar]
  8. FARMER T. A., Jr, HAMMACK W. J., FROMMEYER W. B., Jr Idiopathic recurrent rhabdomyolysis associated with myoglobinuria: report of a case. N Engl J Med. 1961 Jan 12;264:60–66. doi: 10.1056/NEJM196101122640202. [DOI] [PubMed] [Google Scholar]
  9. FITZ T. E. Familial paroxysmal paralytic myoglobinuria. W V Med J. 1957 Jul;53(7):264–270. [PubMed] [Google Scholar]
  10. GILLETT R. L. Primary myoglobinuria. N Engl J Med. 1959 Jun 4;260(23):1156–1160. doi: 10.1056/NEJM195906042602302. [DOI] [PubMed] [Google Scholar]
  11. HAASE G. R., ENGEL A. G. Paroxysmal recurrent rhabdomyolysis. Arch Neurol. 1960 Apr;2:410–419. doi: 10.1001/archneur.1960.03840100048008. [DOI] [PubMed] [Google Scholar]
  12. HOLMGREN A., JONSSON B., LEVANDER M., LINDERHOLM H., SJOSTRAND T., STROM G. Low physical working capacity in suspected heart cases due to inadequate adjustment of peripheral blood flow (vasoregulatory asthenia). Acta Med Scand. 1957 Oct 15;158(6):413–436. doi: 10.1111/j.0954-6820.1957.tb15509.x. [DOI] [PubMed] [Google Scholar]
  13. HOLMGREN A., JONSSON B., SJOSTRAND T. Circulatory data in normal subjects at rest and during exercise in recumbent position, with special reference to the stroke volume at different work intensities. Acta Physiol Scand. 1960 Aug 25;49:343–363. doi: 10.1111/j.1748-1716.1960.tb01957.x. [DOI] [PubMed] [Google Scholar]
  14. HOLMGREN A., MATTSSON K. H. A new ergometer with constant work load at varying pedalling rate. Scand J Clin Lab Invest. 1954;6(2):137–140. doi: 10.3109/00365515409134855. [DOI] [PubMed] [Google Scholar]
  15. HOLMGREN A., STROM G. Blood lactate concentration in relation to absolute and relative work load in normal men, and in mitral stenosis, atrial septal defect and vasoregulatory asthenia. Acta Med Scand. 1959 Mar 4;163(3):185–193. doi: 10.1111/j.0954-6820.1959.tb10399.x. [DOI] [PubMed] [Google Scholar]
  16. HUCKABEE W. E. Control of concentration gradients of pyruvate and lactate across cell membranes in blood. J Appl Physiol. 1956 Sep;9(2):163–170. doi: 10.1152/jappl.1956.9.2.163. [DOI] [PubMed] [Google Scholar]
  17. JAVID J., HOROWITZ H. I., SANDERS A. R., SPAET T. H. Idiopathic paroxysmal myoglobinuria. Report of a case with Med. AMA Arch Intern Med. 1959 Oct;104:628–633. doi: 10.1001/archinte.1959.00270100114020. [DOI] [PubMed] [Google Scholar]
  18. JORGENSEN K., ASTRUP P. Standard bicarbonate, its clinical significance, and a new method for its determination. Scand J Clin Lab Invest. 1957;9(2):122–132. doi: 10.3109/00365515709101210. [DOI] [PubMed] [Google Scholar]
  19. KONTOS H. A., HARLEY E. L., WASSERMAN A. J., KELLY J. J., 3rd, MAGEE J. H. EXERTIONAL IDIOPATHIC PAROXYSMAL MYOGLOBINURIA. EVIDENCE OF A DEFECT IN SKELETAL MUSCLE METABOLISM. Am J Med. 1963 Aug;35:283–292. doi: 10.1016/0002-9343(63)90219-5. [DOI] [PubMed] [Google Scholar]
  20. KOREIN J., CODDON D. R., MOWREY F. H. The clinical syndrome of paroxysmal paralytic myoglobinuria. Report of 2 cases and an analytical review of the literature. Neurology. 1959 Nov;9:767–785. doi: 10.1212/wnl.9.11.767. [DOI] [PubMed] [Google Scholar]
  21. KOSSMANN R. J., CAMP W. A., ENGLE R. L., Jr Idiopathic recurrent rhabdomyolysis with myoglobinuria. Case report, with diagnostic recommendations and demonstration of unusual heme compounds in the urine. Am J Med. 1963 Apr;34:554–564. doi: 10.1016/0002-9343(63)90079-2. [DOI] [PubMed] [Google Scholar]
  22. PEARSON C. M., BECK W. S., BLAHD W. H. Idiopathic paroxysmal myoglobinuria; detailed study of a case including radioisotope and serum enzyme evaluation. AMA Arch Intern Med. 1957 Mar;99(3):376–389. doi: 10.1001/archinte.1957.00260030056006. [DOI] [PubMed] [Google Scholar]
  23. PEARSON C. M., RIMER D. G., MOMMAERTS W. F. A metabolic myopathy due to absence of muscle phosphorylase. Am J Med. 1961 Apr;30:502–517. doi: 10.1016/0002-9343(61)90075-4. [DOI] [PubMed] [Google Scholar]
  24. PHILLIPPI P. J., JONES F. R., KENOYER W. L. Idiopathic paroxysmal myoglobinuria. J Am Med Assoc. 1960 Feb 27;172:907–908. doi: 10.1001/jama.1960.03020090019004. [DOI] [PubMed] [Google Scholar]
  25. PRANKERD T. A. Electrophoretic properties of myoglobin and its character in sickle-cell diseases and paroxysmal myoglobinuria. Br J Haematol. 1956 Jan;2(1):80–83. doi: 10.1111/j.1365-2141.1956.tb06687.x. [DOI] [PubMed] [Google Scholar]
  26. REINER L., KONIKOFF N., ALTSCHULE M. D., DAMMIN G. J., MERRILL J. P. Idiopathic paroxysmal myoglobinuria; report of two cases and evaluation of the syndrome. AMA Arch Intern Med. 1956 May;97(5):537–550. doi: 10.1001/archinte.1956.00250230031004. [DOI] [PubMed] [Google Scholar]
  27. SCHMID R., HAMMAKER L. Hereditary absence of muscle phosphorylase (McArdle's syndrome). N Engl J Med. 1961 Feb 2;264:223–225. doi: 10.1056/NEJM196102022640504. [DOI] [PubMed] [Google Scholar]
  28. SELDINGER S. I. Catheter replacement of the needle in percutaneous arteriography; a new technique. Acta radiol. 1953 May;39(5):368–376. doi: 10.3109/00016925309136722. [DOI] [PubMed] [Google Scholar]
  29. THOMSON W. H., MACLAURIN J. C., PRINEAS J. W. Skeletal muscle glycogenosis: an investigation of two dissimilar cases. J Neurol Neurosurg Psychiatry. 1963 Feb;26:60–68. doi: 10.1136/jnnp.26.1.60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. WHEBY M. S., MILLER H. S., Jr Idiopathic paroxysmal myoglobinuria; report of two cases occurring in sisters. Review of the literature. Am J Med. 1960 Oct;29:599–610. doi: 10.1016/0002-9343(60)90093-0. [DOI] [PubMed] [Google Scholar]
  31. von FELLENBERG, EPPENBERGER H., RICHTERICH R., AEBI H. [The glycolytic erzyme pattern in the liver, kidney, skeletal muscle, heart muscle and brain of rats and mice]. Biochem Z. 1962;336:334–350. [PubMed] [Google Scholar]

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