Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type)
- PMID: 6737009
- DOI: 10.1097/00005072-198407000-00005
Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type)
Abstract
We report five cases of congenital muscular dystrophy with central nervous system involvement of the Fukuyama type (FCMD) in which cerebral cortical dysplasia was not uniform even in the same brain. We have categorized the dysplasia into three major patterns, each with a predictable topography despite individual variations. Cerebellar micropolygyria was localized to the dorsal halves of each hemisphere. Aberrant fascicles of myelinated nerve fibers, closely associated with micropolygyria, were found in the subarachnoid space of the dorsal cerebellar surface in all but one case. We discuss the characteristics of the cortical dysplasia of FCMD, particularly in relation to that of Walker's lissencephaly, pathogenesis, and the relationship between lesions of the central nervous system and skeletal muscle.
Similar articles
-
Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome.Brain Dev. 1993 May-Jun;15(3):182-91. doi: 10.1016/0387-7604(93)90063-e. Brain Dev. 1993. PMID: 8214343
-
Characteristics of neurons and glia in the brain of Fukuyama type congenital muscular dystrophy.Acta Myol. 2008 Jul;27(1):9-13. Acta Myol. 2008. PMID: 19108571 Free PMC article. Review.
-
Cerebellar micropolygyria in Fukuyama congenital muscular dystrophy: observations in fetal and pediatric cases.Brain Dev. 1990;12(6):774-8. doi: 10.1016/s0387-7604(12)80005-2. Brain Dev. 1990. PMID: 2092587
-
Cortical dysplasia in a 23-week fetus with Fukuyama congenital muscular dystrophy (FCMD).Acta Neuropathol. 1987;74(3):300-6. doi: 10.1007/BF00688196. Acta Neuropathol. 1987. PMID: 3314312
-
[Central Nervous Involvement in Patients with Fukuyama Congenital Muscular Dystrophy].Brain Nerve. 2016 Feb;68(2):119-27. doi: 10.11477/mf.1416200361. Brain Nerve. 2016. PMID: 26873231 Review. Japanese.
Cited by
-
Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A).J Neuropathol Exp Neurol. 2020 Sep 1;79(9):998-1010. doi: 10.1093/jnen/nlaa062. J Neuropathol Exp Neurol. 2020. PMID: 32827036 Free PMC article.
-
The changing MR imaging appearance of polymicrogyria: a consequence of myelination.AJNR Am J Neuroradiol. 2003 May;24(5):788-93. AJNR Am J Neuroradiol. 2003. PMID: 12748072 Free PMC article.
-
Congenital muscular dystrophy and severe central nervous system atrophy in two siblings.Acta Neuropathol. 1995;90(6):650-6. doi: 10.1007/BF00318580. Acta Neuropathol. 1995. PMID: 8615088
-
MRI of the brain in muscle-eye-brain (MEB) disease.Neuroradiology. 1994 Aug;36(6):473-6. doi: 10.1007/BF00593687. Neuroradiology. 1994. PMID: 7991095
-
Cortical dysplasia in Fukuyama congenital muscular dystrophy (FCMD): a Golgi and angioarchitectonic analysis.Acta Neuropathol. 1988;76(2):170-8. doi: 10.1007/BF00688101. Acta Neuropathol. 1988. PMID: 2457291
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases