Abstract

Contractures occur early in the course of neuromuscular diseases. They may even be present at birth as in the case of congenital myotonic dystrophy and congenital myopathies. Up till now, contractures were regarded as an exclusion criterion in spinal muscular atrophy (type I SMA), but recently a deletion of the survival motor neuron gene was found in some cases of type I SMA [1, 2]. When multiple joint contractures are present at birth, the term Arthrogryposis is used [3].

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References

  1. Bingham PM, Shen N, Rennert H, Rorke LB, Black AW, Padilla M, Nordgren RE (1997) Artrhogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene. Neurology 49:848–851

    Article  PubMed  CAS  Google Scholar 

  2. Burglen L, Amiel J, Viollet L et al (1996) Survival motor neuron gene deletions in the arthrogryposis multiplex congenital spinal muscular atrophy association. J Clin Invest 98:1130–1132

    Article  PubMed  CAS  Google Scholar 

  3. Hall JG (1997) Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach and general aspects J Pediatr Orthop B 6:159–166

    Article  PubMed  CAS  Google Scholar 

  4. Routon MC (1998) Myopathies congénitales. Dystrophies musculaires congénitales. In: Arthuis M, Dulac O, Mancini J, Pinsard N, Ponsot G (eds) Neurologie Pédiatrique. Flammarion Medecine-Sciences, Paris, pp 802–816

    Google Scholar 

  5. Dubowitz (1978) Muscle disorder in childood. Major problems in clinical pediatrics. Vol XVI, Saunders

    Google Scholar 

  6. Vajsar J, Sloane A, Mac Gregor DL, Ronen DGM, Becker LE, Jay V (1995) Arthrogryposis multiplex congenita due to congenital myasthenic syndrome. Pediatr Neurol 12:237–241

    Article  PubMed  CAS  Google Scholar 

  7. Vignos PJ, Spencer G, Archibald KC (1963) Management of progressive muscular dystrophy of childood. JAMA 184:103–110

    Article  Google Scholar 

  8. Pous JG (1985) Marche et déplacement de l’enfant paralysé. In: Dimeglio A (eds) “L’enfant paralysé: rééducation et appareillage” Problèmes en Médecine de Rééducation. Masson, vol 6, pp 149–155

    Google Scholar 

  9. Vignos PJ (1983) Physical models of rehabilitation in neuromuscular disease. Muscle and Nerve 6:323–338

    Article  PubMed  Google Scholar 

  10. Vignos PJ, Watkins MP (1966) The effect of exercise in muscular dystrophy. JAMA 197:121–126

    Article  Google Scholar 

  11. Urtizberea JA, Gilardeau G (1996) Exercice musculaire et maladies neuromusculaires. In: Pelissier JF, Urtizberea JA (eds) Les maladies neuromusculaires: de la génétique à la réadaptation. Masson, pp 323–327

    Google Scholar 

  12. Iannacone ST, White M, Browne R, Russman B, Buncher R, Samaha FJ (1997) Muscle fatigue in spinal muscular atrophy. J Child Neurol 12:321–326

    Article  Google Scholar 

  13. Ledoux P, Larroque A (1995) Amyotrophies spinales infantiles. Kinésithérapie de l’enfant paralysé. In: Kinesithérapie pédiatrique. Vol 4, Masson pp109–118

    Google Scholar 

  14. Ledoux P, Larroque A (1995) La maladie de Duchenne de Boulogne. Kinésithérapie de l’enfant paralysé. In: Kinesithérapie pédiatrique. Vol 4, Masson pp 119–144

    Google Scholar 

  15. Muray C, Fixsen JA (1997) Management of knee deformity in classical arthrogryposis multiplex congenita (amyoplasia congenita), J Pediatr Orthop B 6:186–191

    Article  Google Scholar 

  16. Beltramo F, Fort D, Dauphin D (1996) Appareillage de marche du myopathe: Réalités et perspectives. In: Pelissier JF, Urtizberea JA (eds) Les maladies neuromusculaires: de la génétique à la réadaptation. Masson, pp 143–150

    Google Scholar 

  17. Carrelet P, Chabrol B, Jouve JL (1998) Association de résine semi-rigide et de résine rigide: application aux orthèses en rééducation et aux pieds bots de l’enfant. In: Dimeglio A (eds) Le pied de l’enfant et de l’adolescent. Coll de Pathologie Locomotrice et de Medecine Orthopedique. Masson, pp356–358

    Google Scholar 

  18. Forst R, Forst J (1995) Importance of lower limb surgery in Duchenne muscular dystrophy Arch Orthop Ttrauma Surg 114:106–111

    Article  CAS  Google Scholar 

  19. Rideau Y, Duport G, Delaubier A et al (1996) Correction précoce des inégalités musculaires dans la myopathie: analyse internationale. In: Pelissier JF, Urtizberea JA (eds) “Les maladies neuromusculaires: de la génétique à la réadaptation”. Masson, pp 156–170

    Google Scholar 

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© 1999 Springer-Verlag France

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Chabrol, B., Carrelet, P., Bollini, G. (1999). Therapy of Muscular Contractures. In: Serratrice, G., Pouget, J., Azulay, JP. (eds) Exercise Intolerance and Muscle Contracture. Springer, Paris. https://doi.org/10.1007/978-2-8178-0855-0_23

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  • DOI: https://doi.org/10.1007/978-2-8178-0855-0_23

  • Publisher Name: Springer, Paris

  • Print ISBN: 978-2-287-59669-8

  • Online ISBN: 978-2-8178-0855-0

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