Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1976 Dec;51(12):974–977. doi: 10.1136/adc.51.12.974

Motor nerve conduction velocity in spinal muscular atrophy of childhood.

A Moosa, V Dubowitz
PMCID: PMC1546166  PMID: 1015851

Abstract

The ulnar and posterior tibial conduction velocities were measured in 29 children with spinal muscular atrophy, 14 of whom had the servere form of the disease. The ulnar nerve velocity was slow in 12 of the 14 severely affected infants, but normal or fast in 11 of 14 children less severely affected. The corresponding results for the posterior tibial nerve were slow velocities in 11 of 12 infants in the severe group and normal or fast in all 11 infants less severely affected. The difficulty in distinguishing infantile spinal muscular atrophy from peripheral neuropathy is emphasized.

Full text

PDF
974

Selected References

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

  1. Buchthal F., Olsen P. Z. Electromyography and muscle biopsy in infantile spinal muscular atrophy. Brain. 1970;93(1):15–30. doi: 10.1093/brain/93.1.15. [DOI] [PubMed] [Google Scholar]
  2. Chaco J. Conduction velocity of motor nerve fibers in progressive spinal atrophy. Acta Neurol Scand. 1970;46(1):119–122. doi: 10.1111/j.1600-0404.1970.tb05610.x. [DOI] [PubMed] [Google Scholar]
  3. Fried K., Emery A. E. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease). Clin Genet. 1971;2(4):203–209. [PubMed] [Google Scholar]
  4. Gamstorp I. Progressive spinal muscular atrophy with onset in infancy or early childhood. Acta Paediatr Scand. 1967 Jul;56(4):408–423. doi: 10.1111/j.1651-2227.1967.tb15400.x. [DOI] [PubMed] [Google Scholar]
  5. Karch S. B., Urich H. Infantile polyneuropathy with defective myelination: an autopsy study. Dev Med Child Neurol. 1975 Aug;17(4):504–511. doi: 10.1111/j.1469-8749.1975.tb03502.x. [DOI] [PubMed] [Google Scholar]
  6. Moosa A., Dubowitz V. Postnatal maturation of peripheral nerves in preterm and full-term infants. J Pediatr. 1971 Dec;79(6):915–922. doi: 10.1016/s0022-3476(71)80184-1. [DOI] [PubMed] [Google Scholar]
  7. Munsat T. L., Woods R., Fowler W., Pearson C. M. Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease. Brain. 1969 Mar;92(1):9–24. doi: 10.1093/brain/92.1.9. [DOI] [PubMed] [Google Scholar]
  8. Pearn J. H., Carter C. O., Wilson J. The genetic identity of acute infantile spinal muscular atrophy. Brain. 1973 Sep;96(3):463–470. doi: 10.1093/brain/96.3.463. [DOI] [PubMed] [Google Scholar]
  9. Raimbault J., Laget P. L'apport de l'électrolyographie au diagnostic de l'amyotrophie spinale infantile de Werdnig-Hoffmann. Pathol Biol (Paris) 1972 Mar;20(5):287–296. [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES