Abstract
Nine children with congenital fibre type disproportion (CFTD) are described. Their muscle biopsies contained type 1 fibres which were smaller than the largest type 2 fibres by at least 13.5%. Attention is drawn to the variable natural history of this disorder which generally carries a good prognosis but may sometimes be associated with fatal respiratory problems. For important therapeutic, genetic, and prognostic reasons CFTD must be distinguished from other conditions with similar histochemical or clinical features.
Full text
PDF








Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brooke M. H., Engel W. K. The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies. Neurology. 1969 Jun;19(6):591–605. doi: 10.1212/wnl.19.6.591. [DOI] [PubMed] [Google Scholar]
- Caille B., Fardeau M., Harpey J. P., Lafourcade J. Hypotonie congénitale avec atteinte élective des fibres musculaires de type I. A propos de deux observations. Arch Fr Pediatr. 1971 Feb;28(2):205–220. [PubMed] [Google Scholar]
- Dubowitz V., Sharrard J. Congenital clubfoot with central core disease of muscle. Proc R Soc Med. 1968 Dec 12;61(12):1258–1260. [PMC free article] [PubMed] [Google Scholar]
- Fardeau M., Harpey J. P., Caille B. Disproportion congénitale des différents types de fibre musculaire, avec petitesse relative des fibres de type I. Documents morphologiques concernant les biopsies musculaires prélevées chez trois membres d'une même famille. Rev Neurol (Paris) 1975 Nov;131(11):745–766. [PubMed] [Google Scholar]
- Farkas-Bargeton E., Aicardi J., Chevrie J. J., Thieffry S. Apport des techniques histoenzymologiques à l'étude des hypotonies congénitales. Rev Neurol (Paris) 1968 Dec;119(6):513–524. [PubMed] [Google Scholar]
- Kinoshita M., Satoyoshi E., Kumagai M. Familial type I fiber atrophy. J Neurol Sci. 1975 May;25(1):11–17. doi: 10.1016/0022-510x(75)90182-3. [DOI] [PubMed] [Google Scholar]
- LARSEN L. J., SCHOTTSTAEDT E. R., BOST F. C. Multiple congenital dislocations associated with characteristic facial abnormality. J Pediatr. 1950 Oct;37(4):574–581. doi: 10.1016/s0022-3476(50)80268-8. [DOI] [PubMed] [Google Scholar]
- Lake B. D., Wilson J. Zebra body myopathy. Clinical, histochemical and ultrastructural studies. J Neurol Sci. 1975 Apr;24(4):437–446. doi: 10.1016/0022-510x(75)90169-0. [DOI] [PubMed] [Google Scholar]
- Serratrice G., Pellissier J. F., Gastaut J. L., Pouget J. Myopathie congénitale avec hypotrophie sélective des fibres de type I. Rev Neurol (Paris) 1975 Nov;131(11):813–816. [PubMed] [Google Scholar]
- Wynne-Davies R., Lloyd-Roberts G. C. Arthrogryposis multiplex congenita. Search for prenatal factors in 66 sporadic cases. Arch Dis Child. 1976 Aug;51(8):618–623. doi: 10.1136/adc.51.8.618. [DOI] [PMC free article] [PubMed] [Google Scholar]