HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

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.
AuthorsK Takada, H Nakamura, J Tanaka
JournalJournal of neuropathology and experimental neurology (J Neuropathol Exp Neurol) Vol. 43 Issue 4 Pg. 395-407 (Jul 1984) ISSN: 0022-3069 [Print] England
PMID6737009 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Brain Diseases (complications, pathology)
  • Cerebellar Diseases (pathology)
  • Cerebral Cortex (pathology)
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Male
  • Muscular Dystrophies (complications, congenital, pathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: