Skip to main content

Skeletal Muscle and Peripheral Nerves

  • Chapter

Abstract

Striated muscle develops from embryonic mesenchyme. Some head and neck muscles are derived from branchial mesenchyme, limb muscles from the condensation of somatic mesenchyme which forms the limb buds, and trunk muscles from the segmented paraxial myotomes. The primordia of most muscles are defined by the end of the 8th week of gestation. At this stage they are composed of groups of myotubes—multinucleate syncytia containing central chains of nuclei surrounded by peripheral basophilic cytoplasm. Myotubes are formed by fusion of myoblasts, their mitotically active predecessors. A few myoblasts remain when the myotubes are formed and these are thought to give rise eventually to the satellite cells which lie alongside the mature muscle fibres and provide a source of myoblastic stem cells from which myonuclei are derived when required for hypertrophic growth or regeneration. Satellite cells can only be identified with certainty by electron microscopy. They are more common in young than adult muscle, their nuclei contributing between 2% and 10% of total muscle nuclei (Landon 1982).

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   74.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Adams RD, de Reuck J (1973) Metrics of muscle. In: Kakulas BA (ed) Basic research in myology. Int Congr Ser, vol 294, part i. Excerpta Medica, Amsterdam, pp 3–11.

    Google Scholar 

  • Afifi AK, Smith JW, Zellweger H (1965) Congenital non-progressive myopathy. Central core disease and nemaline myopathy in one family. Neurology 15: 371–381.

    Article  PubMed  CAS  Google Scholar 

  • Arnon SS, Midura TF, Damus K, Thompson B, Wood RM, Chin J (1979) Honey and other environmental risk factors in infant botulism. J Pediatr 94: 331–336.

    Article  PubMed  CAS  Google Scholar 

  • Arts WF, Bethlem J, Dinemans KP, Eriksson AW (1978) Investigations on the inheritance of nemaline myopathy. Arch Neurol 35: 72–77.

    Article  PubMed  CAS  Google Scholar 

  • Askanas V, Engel WK, Reddy NB, Barth PG, Bethlem J, Krauss DR et al. (1979) X-linked recessive congenital muscle fibre hypotrophy with central nuclei. Abnormalities of growth and adenylate cyclase in muscle tissue cultures. Arch Neurol 36: 604–609.

    Article  PubMed  CAS  Google Scholar 

  • Aylett P (1954) Five cases of acute infective polyneuritis (Guillain-Barré syndrome) in children. Arch Dis Child 29: 531–536.

    Article  PubMed  CAS  Google Scholar 

  • Barth PG, Van Wijngaarden GK, Bethlem J (1975) X-linked myotubular myopathy with fatal neonatal asphyxia. Neurology 25: 531–536.

    Article  PubMed  CAS  Google Scholar 

  • Baskin JL, Soule EH, Mills SD (1950) Poliomyelitis of the newborn: pathologic changes in two cases. Am J Dis Child 80: 10–21.

    PubMed  CAS  Google Scholar 

  • Bobowick AR, Brody JA (1975) Epidemiology of system atrophies. In: Vinken PJ, Bruyn GW (eds) Handbook of clinical neurology, vol 21. North Holland, Amsterdam, pp 3–42.

    Google Scholar 

  • Bowden DH, Groyer RA (1960) The size of muscle fibres in infants and children. Arch Pathol Lab Med 69: 188–189.

    CAS  Google Scholar 

  • Bradley WG, Hudgson P, Larson PF, Papapetropoulos TA, Jenkinson M (1972) Structural changes in the early stages of Duchenne muscular dystrophy. J Neurol Neurosurg Psychiatry 35: 451–455.

    Article  PubMed  CAS  Google Scholar 

  • Brandt S (1950) Werdnig-Hoffman’s infantile progressive muscular atrophy. Ejnar Munksgaards, Copenhagen.

    Google Scholar 

  • Brooke MH (1973) Congenital fibre type disproportion. In: Kakulas BA (ed) Clinical studies in myology. Proceedings of the 2nd international congress on muscle diseases, Perth Australia. Int Congr Ser No 295, part 2. Excerpta Medica, Amsterdam, p 147.

    Google Scholar 

  • Brooke MH, Neville HE (1972) Reducing body myopathy. Neurology 22: 829–840.

    Article  PubMed  CAS  Google Scholar 

  • Bundey S (1972) A genetic study of infantile and juvenile myasthenia gravis. J Neurol Neurosurg Psychiatry 35: 41–51.

    Article  PubMed  CAS  Google Scholar 

  • Burgen ASV, Dickens F, Zatman LJ (1949) The action of botulinum toxin on the neuromuscular junction. J Physiol 109: 10–24.

    PubMed  CAS  Google Scholar 

  • Byers RK, Taft LT (1957) Chronic multiple peripheral neuropathy in childhood. Pediatrics 20: 517–537.

    PubMed  CAS  Google Scholar 

  • Carbonetto S (1984) The extracellular matrix of the nervous system. Trends in Neuroscience 7: 382–387.

    Article  Google Scholar 

  • Carpenter S, Karpati G (1984) Pathology of skeletal muscle. Churchill Livingstone, London.

    Google Scholar 

  • Carpenter S, Karpati G, Rothman S, Watters G, Andermann F (1978) Pathological involvement of primary sensory neurons in Werdnig-Hoffmann disease. Acta Neuropathol (Berl) 42: 91–97.

    Article  CAS  Google Scholar 

  • Cavanagh JB (1984) The problems of neurons with long axons. Lancet I: 1284–1287.

    Article  Google Scholar 

  • Colling-Saltin A-S (1978) Enzyme histochemistry on skeletal muscle of the human foetus. J Neurol Sci 39: 169–185.

    Article  PubMed  CAS  Google Scholar 

  • Crews J, Kaiser KK, Brooke MH (1976) Muscle pathology of myotonia congenita. J Neurol Sci 28: 449–457.

    Article  PubMed  CAS  Google Scholar 

  • Debré R, Thieffry S (1951) Remarques sur le syndrome de Guillain-Barré chez l’enfant (à propos de 32 observations personnelles). Arch Fr Pediatr 8: 357–364.

    PubMed  Google Scholar 

  • Denborough MA, Dennett X, Anderson R McD (1973) Central core disease and malignant hyperthermia. Br Med J I: 272–273.

    Article  Google Scholar 

  • Di Mauro S (1979) Metabolic myopathies. In: Vinken PJ, Bruyn GW (eds) Handbook of clinical neurology, vol 41. North Holland, Amsterdam, pp 175–234.

    Google Scholar 

  • Drachman DB, Banker BQ (1961) Arthrogryposis multiplex congenita. Arch Neurol 5: 77–93.

    Article  PubMed  CAS  Google Scholar 

  • Dubowitz V (1980) The floppy infant. Clinics in developmental medicine No 76. Spastics international medical publications, Heinemann, London.

    Google Scholar 

  • Dubowitz V (1985) Muscle biopsy: a practical approach. Baillière Tindoll, London.

    Google Scholar 

  • Duchen LW (1970) Changes in motor innervation and cholinesterase localisation induced by botulinum toxin in skeletal muscles of the mouse: differences between fast and slow muscles. J Neurol Neurosurg Psychiatry 33: 40–54.

    Article  PubMed  CAS  Google Scholar 

  • Duchen LW, Tonge DA (1973) The effects of tetanus toxin on neuromuscular transmission and on the morphology of motor end plates in slow and fast skeletal muscle of the mouse. J Physiol 228: 157–172.

    PubMed  CAS  Google Scholar 

  • Duchen LW, Stolkin C, Tonge DA (1972) Light and electron microscopic changes in slow and fast skeletal muscle fibres and their motor end-plates in the mouse after the local injection of tetanus toxin. J Physiol 222: 136–137P.

    Google Scholar 

  • Dyck PJ, Thomas PK, Lambert EH (eds) (1984) Peripheral neuropathy. Saunders, Philadelphia.

    Google Scholar 

  • Emery AEH (1977) Muscle histology and creatine kinase levels in the foetus in Duchenne muscular dystrophy. Nature 266: 472–473.

    Article  PubMed  CAS  Google Scholar 

  • Eng GD, Epstein BS, Engel WK, McKay DW, McKay R (1978) Malignant hyperthermia and central core disease in a child with congenital dislocating hips. Arch Neurol 35: 189–197.

    Article  PubMed  CAS  Google Scholar 

  • Engel AG (1967) Pathological reactions of the Z disk. In: Milhorat AT (ed) Exploratory concepts in muscular dystrophy and related disorders. Int Cong Ser No 147. Excerpta Medica, Amsterdam, p 398.

    Google Scholar 

  • Engel AG (1980) Morphologic and immunopathologic findings in myasthenia gravis and in congenital myasthenic syndrome. J Neurol Neurosurg Psychiatry 43: 577–589.

    Article  PubMed  CAS  Google Scholar 

  • Engel AG, Gomez MR, Groover RV (1971) Multicore disease: a recently recognised congenital myopathy associated with multifocal degeneration of muscle fibres. Mayo Clin Proc 46: 666–681.

    PubMed  CAS  Google Scholar 

  • Engel AG, Angelini C, Gomez MR (1972) Fingerprint body myopathy. Mayo Clin Proc 47: 377–388.

    PubMed  CAS  Google Scholar 

  • Engel WK (1970) Selective and nonselective susceptibility of muscle fibre types. A new approach to human neuromuscular disease. Arch Neurol 22: 97–117.

    Article  PubMed  CAS  Google Scholar 

  • Engel WK, Foster JB, Hughes BP, Huxley HE, Mahler R (1961) Central core disease—an investigation of a rare muscle cell abnormality. Brain 84: 167–184.

    Article  PubMed  CAS  Google Scholar 

  • Engel WK, Gold GN, Karpati G (1968) Type 1 fibre hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model. Arch Neurol 18: 435–444.

    Article  PubMed  CAS  Google Scholar 

  • Fardeau M (1982) Congenital myopathies. In: Mastaglia FL, Walton J (eds) Skeletal muscle pathology. Churchill Livingstone, London, pp 161–203.

    Google Scholar 

  • Farkas E, Tomé FMS, Fardeau M, Arsénio-Nunes ML, Dreyfus P, Diebler MF (1974) Histochemical and ultrastructural study of muscle biopsies in three cases of dystrophia myotonica in the newborn child. J Neurol Sci 21: 273–288.

    Article  PubMed  CAS  Google Scholar 

  • Farkas-Bargeton E, Diebler MF, Arsénio-Nunes ML, Wehrlé R, Rosenberg B (1977) Etude de la maturation histochimique, quantitative et ultrastructurale du muscle foetal humaine. J Neurol Sci 31: 245–260.

    Article  PubMed  CAS  Google Scholar 

  • Fenichel GM (1978) Clinical syndromes of myasthenia in infancy and childhood. Arch Neurol 35: 97–103.

    Article  PubMed  CAS  Google Scholar 

  • Fenichel GM, Engel WK (1963) Histochemistry of muscle in infantile spinal muscular atrophy. Neurology 13: 1059–1066.

    Article  PubMed  CAS  Google Scholar 

  • Frank JP, Harati Y, Butler IJ, Nelson TE, Scott CI (1980) Central core disease and malignant hyperthermia syndrome. Ann Neurol 7: 11–17.

    Article  PubMed  CAS  Google Scholar 

  • Gamstorp I (1956) Adynamia epidosica hereditaria. Acta Paediatr Scand [Suppl] 108: 1–126.

    Google Scholar 

  • Goebel HH, Zeman W, De Myer W (1976) Peripheral motor and. sensory neuropathy of early childhood simulating Werdnig-Hoffmann disease. Neuropadiatrics 7: 182–195.

    Article  CAS  Google Scholar 

  • Gruner JE (1966) Anomalies du réticulum sarcoplasmiques et proliferation des tubules dans le muscle d’une paralysie périodique familiales. CR Soc Biol (Paris) 160: 185–195.

    Google Scholar 

  • Gruner JE, Bargeton E (1952) Lésions thalamiques dans la myatonie du nourrisson. Rev Neurol 86: 236–242.

    PubMed  CAS  Google Scholar 

  • Harper PS, Dyken PR (1972) Early onset dystrophia myotonica. Evidence supporting a maternal environmental factor. Lancet II: 53–55.

    Article  Google Scholar 

  • Hers HG (1963) Alpha-glucosidase deficiency in generalised glycogen storage disease (Pompe’s disease). Biochem J 86: 11–16.

    PubMed  CAS  Google Scholar 

  • Hudgson P, Pearce GW, Walton JN (1967) Pre-clinical muscular dystrophy: histopathological changes observed on muscle biopsy. Brain 90: 565–576.

    Article  PubMed  CAS  Google Scholar 

  • Huijing F, van Creveld S, Losekoot G (1963) Diagnosis of generalised glycogen storage disease (Pompe’s disease). J Pediatr 63: 984–987.

    Article  PubMed  CAS  Google Scholar 

  • Hung T-P, Sung S-M, Liang H-C, Landsborough D, Green IJ (1976) Radiculomyelitis following acute haemorrhagic conjunctivitis. Brain 99: 771–790.

    Article  PubMed  CAS  Google Scholar 

  • Illingworth-Brown B, Brown DH (1966) Lack of an α−1, 4 glucan: α−1, 4 glucan 6-glycosyl transferase in a case of type IV glycogenosis. Proc Natl Acad Sci 56: 725–729.

    Article  Google Scholar 

  • Iwata M, Hirano A (1978) Sparing of the Onufrowicz nucleus in sacral anterior horn lesions. Ann Neurol 4: 245–249.

    Article  PubMed  CAS  Google Scholar 

  • Jansen JKS, Van Essen DC, Brown MC (1975) Formation and elimination of synapses in skeletal muscles of rat. Cold Spring Harbor Symp Quant Biol 40: 425–434.

    Article  Google Scholar 

  • Jerusalem F, Engel AG, Gomez MR (1973) Sarcotubular myopathy. A newly recognised benign congenital, familial muscle disease. Neurology 23: 897–906.

    Article  PubMed  CAS  Google Scholar 

  • Karch SB, Urich H (1975) Infantile polyneuropathy with defective myelination: an autopsy report. Dev Med Child Neurol 17: 504–511.

    Article  PubMed  CAS  Google Scholar 

  • Karpati G, Carpenter S, Andermann F (1971) A new concept of childhood nemaline myopathy. Arch Neurol 24: 291–304.

    Article  PubMed  CAS  Google Scholar 

  • Karpati G, Carpenter S, Engel AG, Watters G, Allen J, Rothman S et al. (1975) The syndrome of systemic carnitine deficiency. Clinical, morphologie, biochemical and pathophysiologic features. Neurology 25: 16–24.

    Article  PubMed  CAS  Google Scholar 

  • Kasman M, Bernstein L, Schulman S (1976) Chronic polyradiculoneuropathy of infancy: a report of three cases with familial incidence. Neurology 26: 565–573.

    Article  PubMed  CAS  Google Scholar 

  • Keesey J, Lindstrom J, Cokely A, Herman C (1977) Antiacetylcholine receptor antibody in neonatal myasthenia gravis. New Engl J Med 296: 55.

    PubMed  CAS  Google Scholar 

  • Kennedy WR, Sung JH, Berry JF, Mastri A (1971) Hypertrophic neuropathy with primary failure of peripheral myelination. Trans Am Neurol Assoc 96: 75–79.

    PubMed  CAS  Google Scholar 

  • Kinoshita M, Satoyoshi E, Suzuki Y (1975) Atypical myopathy with myofibrillar aggregates. Arch Neurol 32: 417–420.

    Article  PubMed  CAS  Google Scholar 

  • Lake BD, Wilson J (1975) Zebra body myopathy. Clinical, histochemical and ultrastructural studies. J Neurol Sci 24: 437–446.

    Article  PubMed  CAS  Google Scholar 

  • Landon DN (1982) Skeletal muscle—normal morphology, development and innervation. In: Mastaglia FL, Walton J (eds) Skeletal muscle pathology. Churchill Livingstone, London, pp 1–87.

    Google Scholar 

  • Leibowitz S, Hughes RAC (1983) Immunology of the nervous system. Edward Arnold, London.

    Google Scholar 

  • Lyon G (1969) Ultrastructural study of a nerve biopsy from a case of early infantile chronic neuropathy. Acta Neuropathol (Berl) 13: 131–142.

    Article  CAS  Google Scholar 

  • Mahoney MJ, Haseltine FP, Hobbins JC, Banker BQ, Caskey CT, Golbus MS (1977) Prenatal diagnosis of Duchenne’s muscular dystrophy. New Engl J Med 297: 968–973.

    Article  PubMed  CAS  Google Scholar 

  • Martin L, Joris C (1970) Histoenzymological and semiquantitative study of the maturation of the human muscle fibre. In: Walton JN, Canal N, Scarlato N (eds) Diseases of muscle. Int Congr Series No 199. Excerpta Medica, Amsterdam, p 657.

    Google Scholar 

  • Mastaglia FL, Walton J (1982) Skeletal muscle pathology. Churchill Livingstone, London.

    Google Scholar 

  • Montgomery RD (1962) Growth of human striated muscle. Nature 195: 194–195.

    Article  PubMed  CAS  Google Scholar 

  • Morgan-Hughes JA (1982) Mitochondrial myopathies. In: Mastaglia FL, Walton J (eds) Skeletal muscle pathology. Churchill Livingstone, London, pp 309–339.

    Google Scholar 

  • Mouton CM, Smillie JG, Bower AG (1950) Report of ten cases of poliomyelitis in infants under 6 months of age. J Pediatr 36: 482–492.

    Article  Google Scholar 

  • Namba T, Shapiro MS, Brunner NG, Grob D (1971) Myasthenia gravis occurring in twins. J Neurol Neurosurg Psychiatry 34: 531–534.

    Article  PubMed  CAS  Google Scholar 

  • Nonaka I, Chou S (1979) Congenital muscular dystrophy. In: Vinken PJ, Bruyn GW (eds) Handbook of clinical neurology, vol 41, North Holland, Amsterdam, pp 27–50.

    Google Scholar 

  • Öckerman PA (1965) Glycogen storage disease in Sweden. Acta Paediatr Scand 160: 1–31.

    Google Scholar 

  • Oppenheimer DR (1984) Diseases of the basal ganglia cerebellum and motor neurons. In: Hume Adams J, Corsellis JAN, Duchen LW (eds) Greenfield’s neuropathology, 4th edn. Edward Arnold, London, pp 699–747.

    Google Scholar 

  • Pickett J, Berg B, Chaplin E, Brunstetter-Shafer M (1976) Syndrome of botulism in infancy: clinical and electrophysiological study. New Engl J Med 295: 769–772.

    Article  Google Scholar 

  • Price DL, Griffin JW, Peck K (1977) Tetanus toxin: evidence for binding at presynaptic nerve endings. Brain Res 121: 379–384.

    Article  PubMed  CAS  Google Scholar 

  • Rebouche CJ, Engel AG (1980) Carnitine biosynthesis in systemic carnitine deficiency. Neurology 30: 368.

    Google Scholar 

  • Roses AD, Harper PS, Bossen EG (1979) Myotonic muscular dystrophy. In: Vinken PJ, Bruyn GW (eds) Handbook of clinical neurology, vol 40, pp 485-532.

    Google Scholar 

  • Salafsky IS, Nadler HL (1971) α−1,4-glucosidase activity in Pompe’s disease. J Pediatr 79: 794–798.

    Article  PubMed  CAS  Google Scholar 

  • Salafsky IS, Nadler HL (1973) Deficiency of acid α− glucosidase in urine of patients with Pompe’s disease. J Pediatr 82: 294–297.

    Article  PubMed  CAS  Google Scholar 

  • Sarnat HB (1982) Developmental disorders of muscle. In: Mastaglia FL, Walton J (eds) Skeletal muscle pathology. Churchill Livingstone, London, pp 140–160.

    Google Scholar 

  • Shafiq SA, Dubowitz V, Peterson H de C, Milhorat AT (1967) Nemaline myopathy. Report of a fatal case with histochemical and electron microscopic studies. Brain 90: 817–828.

    Article  PubMed  CAS  Google Scholar 

  • Shelokov A, Weinstein L (1951) Poliomyelitis in the early neonatal period: report of a case with possible intrauterine infection. J Pediatr 38: 80–84.

    Article  PubMed  CAS  Google Scholar 

  • Shy GM, Magee KR (1956) A new congenital non-progressive myopathy. Brain 79: 610–620.

    Article  PubMed  CAS  Google Scholar 

  • Shy GM, Engel WK, Somers JE, Warko T (1963) Nemaline myopathy: a new congenital myopathy. Brain 86: 793–810.

    Article  PubMed  CAS  Google Scholar 

  • Spiro AJ, Shy GM, Gonatas NK (1966) Myotubular myopathy. Persistence of fetal muscle in an adolescent boy. Arch Neurol 14: 1–14.

    Article  PubMed  CAS  Google Scholar 

  • Steiman GS, Rorke LB, Brown MJ (1980) Infantile neuronal degeneration masquerading as Werdnig-Hoffmann disease. Ann Neurol 9: 317–324.

    Article  Google Scholar 

  • Sung JH, Mastri AR (1980) Spinal autonomic neurons in Werdnig-Hoffmann disease, Mannosidosis and Hurler’s syndrome: distribution of autonomie neurons in the spinal cord. J Neuropathol Exp Neurol 39: 441–451.

    Article  PubMed  CAS  Google Scholar 

  • Swash M, Schwartz MS (1984) Biopsy pathology of muscle. Chapman and Hall, London.

    Google Scholar 

  • Taylor PE (1962) Traumatic intradural avulsion of the nerve roots in the brachial plexus. Brain 85: 579–602.

    Article  PubMed  CAS  Google Scholar 

  • Vanier TM (1960) Dystrophia myotonica in childhood. Br Med J II: 1284–1288.

    Article  Google Scholar 

  • Van Wijngaarden GK, Fleury P, Bethlem J, Meijer AEFM (1969) Familial ‘myotubular’ myopathy. Neurology 19: 901–908.

    Article  PubMed  Google Scholar 

  • Vassilopoulos D, Emery AEH (1977) Muscle nuclear changes in fetuses at risk for Duchenne muscular dystrophy. J Med Genet 14: 13–15.

    Article  PubMed  CAS  Google Scholar 

  • Zelena J (1963) Development of muscle receptors after tenotomy. Physiol Bohemoslov 12: 30–36.

    PubMed  CAS  Google Scholar 

  • Zelena J (1975) The role of sensory innervation in the development of mechanoreceptors. In: Iggo A, Ilyinsky OB (eds) Somatosensory and visceral receptor mechanisms. Elsevier, Amsterdam, p 59.

    Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1987 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Esiri, M.M. (1987). Skeletal Muscle and Peripheral Nerves. In: Keeling, J.W. (eds) Fetal and Neonatal Pathology. Springer, London. https://doi.org/10.1007/978-1-4471-3523-4_25

Download citation

  • DOI: https://doi.org/10.1007/978-1-4471-3523-4_25

  • Publisher Name: Springer, London

  • Print ISBN: 978-1-4471-3525-8

  • Online ISBN: 978-1-4471-3523-4

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics