Congenital fiber-type disproportion myopathy with type I fiber predominance and type II fiber smallness and atrophy--a sterological analysis
- PMID: 15696781
Congenital fiber-type disproportion myopathy with type I fiber predominance and type II fiber smallness and atrophy--a sterological analysis
Abstract
Congenital myopathy with fiber-type disproportion is an established disorder, where type I fibers predominate with smallness of the same type. We report a family with three siblings (12-year-old boy, 9-year-old girl, and 6-year-old boy) with clinical features of congenital myopathy, where muscle biopsy in the eldest sib showed fiber-type disproportion. Type I fibers predominated with small and atrophic type II fibers which is unusual, especially when the child did not have any other clinical or biochemical abnormality to account for this type of variation. Further, a stereological analysis highlighted the differences with regards to number, size and even volume of the fiber types. A 3-dimensional concept is proposed for this morphological abnormality.
Similar articles
-
Clinical and histologic changes in the follow-up of a congenital myopathy.Pediatr Neurol. 2005 Aug;33(2):139-41. doi: 10.1016/j.pediatrneurol.2005.02.012. Pediatr Neurol. 2005. PMID: 16087062
-
Congenital muscle fiber-type disproportion in a patient with congenital central hypoventilation syndrome due to PHOX2B mutations.J Child Neurol. 2008 Jul;23(7):829-31. doi: 10.1177/0883073808314895. J Child Neurol. 2008. PMID: 18658083
-
Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases.Neurol India. 2004 Jun;52(2):254-6. Neurol India. 2004. PMID: 15269486
-
Congenital fiber-type disproportion.Semin Pediatr Neurol. 2011 Dec;18(4):264-71. doi: 10.1016/j.spen.2011.10.008. Semin Pediatr Neurol. 2011. PMID: 22172422 Review.
-
Muscle type and fiber type specificity in muscle wasting.Int J Biochem Cell Biol. 2013 Oct;45(10):2191-9. doi: 10.1016/j.biocel.2013.05.016. Epub 2013 May 21. Int J Biochem Cell Biol. 2013. PMID: 23702032 Review.