. Author manuscript; available in PMC: 2017 Jul 22.

Published in final edited form as: J Med Genet. 2011 Mar 25;48(6):396–406. doi: 10.1136/jmg.2010.087528

Table 2.

Brain imaging data for patients with deletion 14q12 or FOXG1 mutations

	This report N=11	Literature N=15 (ref. 1–5,9–13)
Simplified gyral pattern (SIMP)	11/11 SIMP	01/01 SIMP
Pachygyria, mild frontal	03/11 frontal pachygyria	00/02 frontal pachygyria
Reduced volume white matter (frontal)	11/11 reduced WM	04/04 reduced WM
Hypogenesis corpus callosum (frontal)	09/11 hypogenesis CC	09/09 hypogenesis CC
Agenesis corpus callosum (severe)	01/11 ACC with deletion	02/13 ACC

Abbreviations: ACC, agenesis of corpus callosum; CC, corpus callosum; SIMP, simplified gyral pattern; WM, white matter