ARE THE MUSCULAR DYSTROPHIES NEUROGENIC?*
1974; Wiley; Volume: 228; Issue: 1 Linguagem: Inglês
10.1111/j.1749-6632.1974.tb20513.x
ISSN1749-6632
Autores Tópico(s)Mitochondrial Function and Pathology
ResumoAnnals of the New York Academy of SciencesVolume 228, Issue 1 p. 244-260 ARE THE MUSCULAR DYSTROPHIES NEUROGENIC?* Lewis P. Rowland, Lewis P. Rowland Spiller Neurological Unit Hospital of the University of Pennsylvania Philadelphia, Pennsylvania 19104 Neurological Institute, Columbia-Presbyterian Medical Center, 710 West 168th St., New York, New York, 10032.Search for more papers by this author Lewis P. Rowland, Lewis P. Rowland Spiller Neurological Unit Hospital of the University of Pennsylvania Philadelphia, Pennsylvania 19104 Neurological Institute, Columbia-Presbyterian Medical Center, 710 West 168th St., New York, New York, 10032.Search for more papers by this author First published: March 1974 https://doi.org/10.1111/j.1749-6632.1974.tb20513.xCitations: 20 * This study was supported by USPHS Grant NS 08075 and a grant from the Muscular Dystrophy Associations of America. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Harris, J. B. 1971. The relation of trophic influences to diseases of muscle. Dev. Med. Child. Neurol. 13: 669–671. 2 Dubowitz, V. 1971. Muscular dystrophy—Where is the lesion? Dev. Med. Child. Neurol. 13: 238–240. 3 Bradley, W. G. 1971. Nerve, muscle and muscular dystrophy. Dev. Med. Child. Neurol. 13: 528–530. 4 Goldblatt, D. 1969. Motor neuron disease: historical introduction. In Motor Neuron Diseases. F. H. Norris & I. T. Kurland, Eds.: 1–11. Grune & Stratton. New York , N.Y . 5 Aran, F. A. 1850. Recherches sun une maladic non encore décrite du système musculaire (atrophic musculaire progressive). Arch. Gen. Med. 24: 5–35, 172–214. 6 Meyron, E. 1852. On granular and fatty degeneration of the voluntary muscles. Med. Chir. Trans. 35: 73–84. 7 Duchenne, G. B. 1855, 1861, 1872. De l'électrisation localisée et son application à la pathologic, et à la thérapeutique. 1st, 2nd, & 3rd edits. Baillière et Fils. Paris , France . 8 Eulenberg, A. & R. Conheim. 1866. Ergebnisse der anatomischen Untersuchung eines Falles von sogennanter Muskelhypertrophie. Verh. Berl. Med. Ges. 1: 191–210. 9 Griesinger, W. 1865. Über Muskelhypertrophie. Arch. Heilk. 6: 1–13. 10 Duchenne, G. B. 1868. Recherches sur le paralysie musculaire pseudohypertrophique ou paralysic myo-sclerosique. Arch. Gen. Med. 11: 5–25, 179–209, 305–321, 421–443, 522–588. 11 Landouzy, L. J., & Dejerine. 1886. Nouvelles recherches cliniques et anatomo-pathologiques sur la myopathie atrophique progressive a propos de six observations nouvelles, dont une avec autopsie. Rev. Med. 6: 977–1027. 12 Gibney, V. P. 1886. Is there a primary cord lesion in pseudohypertrophic paralysis? J. Nerv. Ment. Dis. 13: 572–574. 13 Middleton, G. S. 1884. On the pathology of pseudohypertrophic muscular paralysis, with remarks on a so-called degeneration of the nervous system. Glasgow Med. J. 22: 81–106. 14 Pekelharing, C. A. 1882. Ein Fall von Rückenmarkserkrankung bei Pscudomuskelhypertrophique. Virchows Arch. (Pathol. Anat.) 89: 228–235. 15 Schultze, F. 1886. Über den mit Hypertrophie verbundenen piogressiven Muskel-schwund und ähnlichc Krankheitsformen. Bergmann. Wiesbaden , Germany . 16 Collins, J. 1895. A contribution to the pathology and morbid anatomy of amyotrophic lateral sclerosis. J. Nerv. Ment. Dis. 22: 688–692. 17 Charcot, J. M. 1874. De la sclerose laterale amyotrophique. Prog. Med. 2: 325–327, 341–342, 453–455. 18 Erb, W. 1891. Dystrophia muscularis progressive. Klinische und pathologisch-anatomische Studien. Dtsch. Z. Nervenh. 1: 13–94, 173–261. 19 Ballet, G. & Laignel-Lavastine. 1908. Myopathie ancienne avec disparition d'un grand nombre des cellules radiculaires antérieures. Encéphale 3: 229–251. 20 Friesz, J. 1930. Beitrag zur anatomichen Kenntnis der Muskeldystrophie. Dtsch. Z. Nervenh. 112: 318–326. 21 Frohmaier, G. 1886. Über progressive Muskelatrophie. Dtsch. Med. Wochenschr. 12: 394–396, 410–412. 22 Grundmann, E. & R. Beckmann. 1962. Zur pathologischen Anatomie der Dystrophia musculorum progressive Erb. Beitr. Pathol. 127: 335–350. 23 Lorenz, H. 1904. Die Muskelerkrankungen. Holder. Vienna , Austria . 24 Milhorat, A. T. & H. G. Wolff. 1943. Studies in deases of muscle. III. Progressive muscular dystrophy of atrophic distal type; report on a family; report of autopsy. Arch. Neurol. Psychiat. 49: 655–664. 25 Stiller, W. G. 1907. Myopathy of the distal type and its relation to the neural form of muscular atrophy (Charcot-Marie-Tooth type). J. Nerv. Ment. Dis. 34: 14–30. 26 Biemond, A. 1955. Myopathia distails juvenilis hereditaria. Acta Psychiat. Neurol. Scand. 30: 25–38. 27 Slauck, A. 1936. Pathologische Anatomie der Myopathien. In Handbuch der Neurologie. O. Bumke & O. Foerster, Eds. Vol. 16: 421–431. Springer-Verlag. Berlin , Germany . 28 Heyck, H. & G. Laudahn. 1969. Die progressiv-dystrophischen Myopathien: 103–104. Springer-Verlag. Berlin , Germany . 29 Hurwitz, S. 1936. Primary myopathies. Arch. Neurol. Psychiat. 36: 1294–1316. 30 Shank, R. E., H. Gilder & C. L. Hoagland. 1944. Studies on diseases of muscle. I. Progressive muscular dystrophy: a clinical review of 40 cases. Arch. Neurol. Psychiat. 52: 431–442. 31 Walton, J. N. & F. J. Nattrass. 1954. On the classification, natural history, and treatment of the myopathies. Brain 77: 169–231. 32 Greenfield, J. G., G. M. Shy, E. C. Alvord & L. Berg. 1957. An Atlas of Muscle Pathology in Neuromuscular Diseases. Livingston. Edinburgh , Scotland . 33 Adams, R. D., D. Denny-Brown & C. M. Pearson. 1962. Diseases of Muscle. 2nd edit. Paul B. Hoeber. New York , N.Y . 34 Engel, W. K. 1962. The essentiality of histo and cyotochemical studies of skeletal muscle in the investigation of neuromuscular disease. Neurology 12: 778–794. 35 Buchthal, F. & S. Clemmsen. 1941. On the differentiation of muscular atrophy by electromyography. Acta Psychiat. Neurol. Scand. 16: 143–181. 36 Kugelberg, E. 1947. Electromyogram in muscular disorders. J. Neurol. Neurosurg. Psychiat. 10: 122–133. 37 Kugelberg, E. 1949. Electromyography in muscular dystrophies with special regard to the differential diagnosis. J. Neurol. Neurosurg. Psychiat. 12: 129–136. 38 Hodes, R., M. G. Larabee & W. J. German. 1948. The human electromyogram in response to nerve stimulation and the conduction velocity of motor axones. Arch. Neurol. Psychiat. 60: 340–365. 39 Eaton, L. M. & E. H. Lambert. 1957. Electromyography and electric stimulation of nerves in diseases of the motor unit. J.A.M.A. 163: 117–1124. 40 Gilliatt, R. W. 1966. Nerve conduction in human and experimental myopathies. Proc. Roy. Soc. Med. 59: 989–993. 41 Schapira, G., J. C. Dreyfus & F. Schapira. 1953. L'élévation du taux de l'aldolase sérique: Test biochimique de myopathies. Sem. Hôp. Paris 29: 1917–1920. 42 Anderson, P. J., S. K. Song & P. Slotwiner. 1967. The muscle biopsy program at Mount Sinai Hospital: results of a 5-year prospective study. J. Mt. Sinai Hosp. 36: 171–205. 43 Brooke, M. H. & W. K. Engel. 1966. The histologic diagnosis of neuromuscular disease: a review of 79 biopsies. Arch. Phys. Med. Rehabil. 47: 99–121. 44 Humphrey, J. E. & G. M. Shy. 1962. Diagnostic electromyography: clinical and pathological correlation in neuromuscular disorders. Arch. Neurol. 6: 339–352. 45 Hausmanowa-Petrusewicz, I., B. Emeryk, B. Wasowicz & A. Kopec. 1967. Electromyography in neuromuscular diagnostics. Electromyography 7: 203–225. 46 Hausmanowa-Petrusewicz, J. & H. Jedrzedowska. 1971. Correlation between electromyographic findings and muscle biopsy in cases of neuromuscular disease. J. Neurol. Sci. 13: 85–106. 47 Schwarz, R. A., K. C. Archibald & J. W. C. Hagstron. 1966. Correlative findings by electromyography and muscle biopsy in neuromuscular disorders. Arch. Phys. Med. 47: 653–658. 48 Bhatt, G. P., J. T. Black, D. L. Schotland & P. V. Dejesus. Diagnostic accuracy of quantitative electromyography and histochemistry: 104 cases. In preparation. 49 Kugelberg, E. & L. Welander. 1956. Heredofamilial juvenile muscular atrophy simulating muscular dystrophy. Arch. Neurol. Psychiat. 75: 500–509. 50 Zellweger, H., A. Afiffi, W. F. McCormick & W. Mergner. 1967. Severe congenital muscular dystrophy. Am. J. Dis. Child. 114: 591–602. 51 Zellweger, H. & W. F. McCormick. 1968. Scapuloperoneal dystrophy and scapuloperoneal atrophy. Helv. Paediatr. Acta 23: 643–649. 52 Drachman, D. B., S. R. Murphy, M. P. Nigam & J. R. Hills. 1967. "Myopathic" changes in chronically denervated muscle. Arch. Neurol. 16: 14–24. 53 Haase, G. R. & G. M. Shy. 1960. Pathological changes in muscle biopsies from patients with peroneal muscular atrophy. Brain 83: 631–637. 54 Van Wijngaarden, G. & J. Bethlem. 1973. Benign infantile spinal muscular atrophy. A prospective study. Brain 96: 163–170. 55 Panitch, H. S. & G. M. Franklin. 1972. Elevation of serum creatine phosphokinase in amyotrophic lateral sclerosis. Neurology 22: 964–966. 56 Hetnarska, L., J. Prot & E. Sawicka. 1968. Creatine phosphokinase activity in spinal muscular atrophy. J. Neurol. Sci. 6: 261–267. 57 Koufen, H. & U. Consbruch. 1970. Die Serum-Creatin Phosphokinase (CPK) Aktivität bei amyotropher Lateralsklerose (ALS) und anderen neurogen Muskel-trophien unter Berücksichtigung differential diagnostischer Aspekte. Nervenartz 41: 509–603. 58 Wohlfart, G. 1942. Zwei Falle von Dystrophia musculorum progressiva mit fibrillaren Zuckungen und atypischen Muskelbefund. Dtsch. Z. Nervenh. 153: 189–204. 59 Rowland, L. P., D. L. Schotland, R. E. Lovelace & R. B. Layzer. 1967. Neurogenic muscular atrophies. In Exploratory Concepts in Muscular Dystrophy. A. T. Milhorat, Ed.: 41–48. Excerpta Med. Found. Amsterdam , The Netherlands . 60 Zellweger, H. & H. J. Schneider. 1968. Syndrome of hypotonia-hypomenia-hypogonadism-obesity (HHHO) or Prader-Willi Syndrome. Am. J. Dis. Child. 115: 588–598. 61 Buller, A. J., J. C. Eccles & R. M. Eccles. 1960. Interactions between motoneurones and muscles in respect of the characteristic speeds of their contraction. J. Physiol. 193: 417–439. 62 Allen, J. E. & D. W. Rodgin. 1960. Mental retardation in association with progressive muscular dystrophy. Am. J. Dis. Child. 100: 208–211. 63 Cohen, H. J., G. E. Molnar & L. T. Taft. 1968. The genetic relationship of progressive muscular dystrophy (Duchenne type) and mental retardation. Develop. Med. Child Neurol. 10: 754–765. 64 Dubowitz, V. 1965. Intellectual impairment in muscular dystrophy. Arch. Dis. Child. 40: 296–301. 65 Dubowitz, V. & L. Crome. 1969. The central nervous system in Duchenne muscular dystrophy. Brain 92: 805–808. 66 Giannini, G. & M. Marcheschi. 1959. Sui distrubi psichici hella distrofia musculare primitiva. Sist. Nerv. 11: 461. 67 Morrow, R. S. & J. Cohen. 1954. The psychosocial factors in muscular dystrophy. J. Child. Psychiat. 3: 70–80. 68 Prosser, E. J., E. G. Murphy & M. W. Thompson. 1969. Intelligence and the gene for Duchenne muscular dystrophy. Arch. Dis. Child. 44: 221–230. 69 Kayser-Gatchalian, M. C. 1971. Intelligengschwache und progressive Muskeldys-trophie vom Duchenne-Typ. Nervenarzt 42: 575–579. 70 Prot, J. 1971. Clinical studies in progressive muscular dystrophy. Pol. Med. J. 11: 1004–1012. 71 Rosman, N. P. 1970. The cerebral defect and myopathy in Duchenne muscular dystrophy. Neurology 20: 329–335. 72 Rosman, N. P. & B. A. Kakulas. 1962. Mental deficiency associated with muscular dystrophy—a neuropathological study. Brain 89: 968–977. 73 Truitt, C. J. 1955. Personal and social adjustments of children with muscular dystrophy. Am. J. Phys. Med. 34: 124–128. 74 Worden, D. K. & P. J. Vignos, Jr. 1962. Intellectual function in childhood progressive muscular dystrophy. Pediatrics 29: 968–977. 75 Zellweger, H. & E. Niedermeyer. 1965. Central nervous system manifestations in childhood muscular dystrophy. I. Psychometric and electroencephalographic findings. Ann. Pediatr. 205: 25–42. 76 Caspary, E. A., S. Currie & E. J. Field. 1971. Sensitized lymphocytes in muscular dystrophy: evidence for a neural factor in pathogenesis. J. Neurol. Neurosurg. Psychiat. 34: 353–356. 77 Engel, W. K. 1970. Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases. Arch. Neurol. 22: 97–117. 78 Fenichel, G. M., W. B. Kibler, W. H. Olson & W. D. Dettbarn. 1972. Chronic inhibition of cholinesterase as a cause of myopathy. Neurology 22: 1026–1032. 79 Skeate, Y., A. Bishop & V. Dubowitz. 1969. Differentiation of diseased human muscle in culture. Cell Tissue Kinet. 2: 307–310. 80 Gallup, B., A. Bishop & V. Dubowitz. 1972. Autoradiographic studies of RNA and DNA synthesis during myogenesis in cultures of human, chick, and rat muscle. J. Neurol. Sci. 17: 127–140. 81 Gallup, B., H. Strugalska-Cynowska & V. Dubowitz. 1972. Histochemical studies on normal and diseased human and chick muscle in tissue culture. J. Neurol. Sci. 17: 109–125. 82 Bishop, A., B. Gallup, Y. Skeate & V. Dubowitz. 1971. Morphological studies on normal and diseased muscle. J. Neurol. Sci. 13: 333–350. 83 Kakulas, B. A., J. M. Papadimitriou, J. O. Knight & F. L. Mastaglia. 1968. Normal and abnormal human muscle in tissue culture. Proc. Aust. Assoc. Neurol. 5: 79–85. 84 McComas, A. J., P. R. W. Fawcett, M. J. Campbell & R. E. P. Sica. 1971. Electrophysiological estimation of the number of motor units within a human muscle. J. Neurol. Neurosurg. Psychiat. 34: 121–131. 85 McComas, A. J., R. E. P. Sica & J. C. Brown. 1971. Myasthenia gravis: evidence for a “central” defect. J. Neurol. Sci. 13: 107–113. 86 McComas, A. J., R. E. P. Sica & M. J. Campbell. 1971. "Sick" motoneurones. A unifying concept of muscle disease. Lancet 1: 321–325. 87 McComas, A. J., R. E. P. Sica & S. Currie. 1970. Muscular dystrophy: myopathy or neuropathy? Lancet 1: 1119. 88 McComas, A. J., R. E. P. Sica & S. Currie. 1970. Muscular dystrophy: evidence for a neural factor. Nature 226: 1263–1264. 89 McComas, A. J., R. E. P. Sica & S. Currie. 1971. An electrophysiological study of Duchenne dystrophy. J. Neurol. Neurosurg. Psychiat. 34: 461–468. 90 McComas, A. J. & H. C. Thomas. 1968. A study of the muscle twitch in the Duchenne type muscular dystrophy. J. Neurol. Sci. 7: 309–312. 91 McComas, A. J., M. J. Campbell & R. E. P. Sica. 1971. Electrophysiological study of dystrophia myotonica. J. Neurol. Neurosurg Psychiat 34: 132–139. 92 Sica, R. E. P. & A. J. McComas. 1971. An electrophysiological investigation of limb-girdle and facioscapulohumeral dystrophy. I. Neurol. Neurosurg. Psychiat. 34: 469–474. 93 Hathaway, P. W., W. K. Engel & H. Zellweger. 1970. Experimental myopathy after microarterial embolization: comparison with childhood X-linked pseudo-hypertrophic muscular dystrophy. Arch. Neurol. 22: 365–378. 94 Mendell, J. R., W. K. Engel & E. C. Derber. 1971. Duchenne muscular dystrophy: functional ischemia reproduces its characteristic lesions. Science 172: 1143–1145. 95 Emery, A. E. H. & J. L. Schelling. 1964. Limb blood flow in patients and carriers of Duchenne muscular dystrophy. Acta Genet. 15: 337–344. 96 Warmolts, J. R. & W. K. Engel. 1970. A critique of the “myopathic” electromyogram. Trans. Am. Neurol. Assoc. 95: 175–177. 97 Welander, L. 1947. Neostigmine as a diagnostic test in progressive muscular atrophy and dystrophy. Arch. Psychiat. Neurol. Scand. Suppl. 46: 329–336. 98 Patel, A. M. & R. K. Swami. 1969. Muscle percussion and neostigmine test in the clinical evaluation of neuromuscular disorders. N. Engl. J. Med. 281: 523–526. 99 Pinelli, P. & F. Buchthal. 1953. Muscle action potentials in myopathies with special regard to progressive muscular dystrophy. Neurology 3: 347–359. 100 Buchthal, F. & P. Pinelli. 1953. Action potentials in muscular atrophy of neurogenic origin. Neurology 3: 591–603. 101 Buchthal, F., P. Rosenfalck & F. Erminio. 1960. Motor unit territory and fiber density in myopathies. Neurology 10: 398–408. 102 Erminio, F., F. Buchthal & P. Rosenfalck. 1959. Motor unit territory and muscle fiber concentration in paresis due to peripheral nerve injury and anterior horn cell involvement. Neurology 9: 656–671. 103 Farmer, T. W., F. Buchthal & P. Rosenfalck. 1959. Refractory and irresponsive periods in progressive muscular dystrophy and paresis due to lower motor neurone involvement. Neurology 9: 747–756. 104 Hausmanowa-Petrusewicz, I., J. Prot, Niebros-Doboszi, L. Hetnarska, B. Emeryk, B. Wasowicz, W. Askansas & C. Slucka. 1968. Studies of healthy relatives of patients with Duchenne muscular dystrophy. J. Neurol. Sci. 7: 465–480. 105 Kozicka, A., J. Prot & R. Wasilewski. 1971. Mental retardation in patients with Duchenne progressive muscular dystrophy. J. Neurol. Sci. 14: 209–213. 106 Jennekens, F. G., B. E. Tomlinson & J. N. Walton. 1971. Histochemical aspects of limb muscles in old age. An autopsy study. J. Neurol. Sci. 14: 259–276. 107 Jennekens, F. G., B. E. Tomlinson & J. N. Walton. 1972. The extensor digitorum brevis: histological and histochemical aspects. J. Neurol. Neurosurg. Psychiat. 35: 124–132. 108 Rosenberg, R. N., D. L. Schotland, R. E. Lovelace & L. P. Rowland. 1968. Progressive ophthalmoplegia. Arch. Neurol. 19: 362–376. 109 Drachman, D. A., N. Wetzel, M. Wasserman & H. Naito. 1969. Experimental denervation of ocular muscles. A critique of “ocular myopathy.” Arch. Neurol. 21: 170–175. 110 Mulder, D. W., R. A. Rosenbaum & D. D. Layton, Jr. 1972. Late progression of poliomyelitis or forme fruste amyotrophic lateral sclerosis. Mayo Clin. Proc. 47: 756–762. 111 Kondo, K. & T. Tusubaki. 1970. Facio-scapulo-humeral muscular dystrophy in a patient with one paretic leg due to poliomyelitis. J. Neurol. Sci. 10: 1–10. 112 Brown, H. D., S. K. Chattopadhyay & A. B. Patel. 1967. Erythrocyte abnormality in human myopathy. Science 157: 1577–1578. 113 Peter, J. B., M. Worsfold & C. M. Pearson. 1969. Erythrocyte ghost adenosine triphosphatase in Duchenne dystrophy. J. Lab. Clin. Med. 74: 103–108. 114 Araki, S. & S. Maw atari. 1971. Ouabain and erythrocyte-ghost adenosine triphosphatase effects in human muscular dystrophies. Arch. Neurol. 24: 187–190. 115 Klassen, G. A. & R. Blostein. 1969. Adenosine triphosphatase and myopathy. Science 163: 492–493. 116 Porterfield, J. L., Y. Wang & A. H. L. Fromm. 1972. Cation transport in Duchenne muscular dystrophy erythrocytes. Proc. Soc. Exp. Biol. Med. 141: 479–481. 117 Schwarzmeier, J., K. Moser & A. Lujf. 1971. Pyruvatkinase-Mangel der Erythrocyten bei hereditärer Myopathie. Klin. Wschr. 49: 156–158. 118 Bosia, A., G. P. Pescarmona & P. Arese. 1971. Red cell glycolysis in the myodys-trophic child. Europ. J. Clin. Invest. 1: 413–420. 119 Perloff, J. K., W. C. Roberts, A. C. Deleon, Jr. & D. O'Doherty. 1967. The distinctive electrocardiogram of Duchenne's progressive muscular dystrophy. An electrocardiographic pathologic correlative study. Am. J. Med. 42: 179–188. 120 Slucka, C. 1968. The electrocardiogram in Duchenne progressive muscular dystrophy. Circulation 38: 933–940. 121 Emery, A. E. H. 1969. Abnormalities of the electrocardiogram in female carriers of Duchenne muscular dystrophy. Brit. Med. J. 2: 418–420. 122 Durkin, H. E., J. H. Ziska & H. Zellweger. 1971. Observations on the electrocardiogram in Duchenne's progressive muscular dystrophy. Helv. Paediat. Acta 26: 331–339. 123 Roman, J. A., Jr., J. K. Perloff, P. J. Bowen & O. Mann. 1972. The vectorcardiogram in Duchenne's progressive muscular dystrophy. Am. Heart J. 84: 588–596. 124 Vogel, P. 1966. Wilhelm Erb und sein Beitrag zu der Lehre von den Myopathies. In Progressive Muskeldystrophie, Myotonia, Myasthenie. E. Kuhn. Ed.: 4. Springer-Verlag. Berlin , Germany . Citing Literature Volume228, Issue1Trophic Function of the NeuronMarch 1974Pages 244-260 ReferencesRelatedInformation
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