Congenital Myotonic Dystrophy
- 1 November 1980
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 37 (11) , 693-696
- https://doi.org/10.1001/archneur.1980.00500600041006
Abstract
• Histometric data on muscle fiber types were studied in two cases of congenital myotonic dystrophy (CMD); one underwent biopsy at the age of 5 months and the other at the age of 10 years. A previously unreported severe deficiency of type IIB fibers were found in both cases. In addition, in the first case, there was type I fiber preponderance and hypotrophy as described in cases of congenital fiber type disproportion (CFTD). It is suggested that an abnormality of motor unit maturation may be common to CMD and to CFTD, and that this results from a disorder of neural trophic influences during muscle development.This publication has 8 references indexed in Scilit:
- Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports.Archives of Disease in Childhood, 1979
- Delay in the maturation of muscle fibers in infants with congenital hypotoniaJournal of the Neurological Sciences, 1978
- Muscle pathology of myotonia congenitaJournal of the Neurological Sciences, 1976
- Maturational Arrest of Fetal Muscle in Neonatal Myotonic DystrophyArchives of Neurology, 1976
- Clinical Effects of Myotonic Dystrophy on Pregnancy and the NeonateArchives of Neurology, 1976
- Pathogenesis of Muscular DystrophiesArchives of Neurology, 1976
- Congenital dystrophia myotonicaNeurology, 1973
- Orthogonal Diameters in the Analysis of Muscle Fibre Size and FormNature, 1963