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Focal cortical dysplasia of Taylor MeSH Supplementary Concept Data 2025


MeSH Supplementary
Focal cortical dysplasia of Taylor
Unique ID
C537067
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537067
Entry Term(s)
Cortical Dysplasia of Taylor with Balloon Cells
Cortical dysplasia of Taylor
FCDT
Focal Cortical Dysplasia of Taylor, Type IIa
Focal Cortical Dysplasia of Taylor, Type IIb
Focal Cortical Dysplasia, Type II
Focal cortical dysplasia, type 2
Registry Numbers
0
Previous Indexing
Malformations of Cortical Development (2010-2014)
Heading Mapped to
*Epilepsy
*Malformations of Cortical Development, Group I
Frequency
199
Note
A cerebral developmental malformation that results in intractable EPILEPSY usually requiring surgery. FCDT is classified histologically into 2 subtypes: a type without balloon cells (Type IIA); and a type with balloon cells (Type IIB). Germline mutations in the TSC1 gene have been identified. OMIM: 607341
Date of Entry
2010/08/25
Revision Date
2015/08/18
Focal cortical dysplasia of Taylor Preferred
Focal Cortical Dysplasia of Taylor, Type IIa Narrower
Focal Cortical Dysplasia of Taylor, Type IIb Narrower
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