MRI analysis of sulcation morphology in polymicrogyria
Anthony James Barkovich,
Anthony James Barkovich
Department of Radiology and Molecular Imaging, University of California, San Francisco, California, U.S.A.
Search for more papers by this authorAnthony James Barkovich,
Anthony James Barkovich
Department of Radiology and Molecular Imaging, University of California, San Francisco, California, U.S.A.
Search for more papers by this authorAddress correspondence to A. J. Barkovich, Department of Radiology and Molecular Imaging, University of California, San Francisco, 505 Paranassus Avenue, Box 0628, San Francisco, CA 94143-0628, U.S.A. E-mail: [email protected]

References
- Barkovich AJ, Kjos BO. (1992) Non-lissencephalic cortical dysplasia: correlation of imaging findings with clinical deficits. AJNR Am J Neuroradiol 13: 95–103.
- Barkovich AJ, Linden CL. (1994) Congenital cytomegalovirus infection of the brain: imaging analysis and embryologic considerations. AJNR Am J Neuroradiol 15: 703–715.
- Barkovich AJ, Hevner R, Guerrini R. (1999) Syndromes of bilateral symmetrical polymicrogyria. AJNR Am J Neuroradiol 20: 1814–1821.
- Bingham PM, Lynch D, Mcdonald-Mcginn D, Zackai E. (1998) Polymicrogyria in chromosome 22 deletion syndrome. Neurology 51: 1500–1502.
- Chang BS, Piao X, Giannini C, Cascino GD, Scheffer I, Woods CG, Topcu M, Tezcan K, Bodell A, Leventer RJ, Barkovich AJ, Grant PE, Walsh CA. (2004) Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation. Neurology 62: 1722–1728.
- Chang BS, Apse KA, Caraballo R, Cross JH, Mclellan A, Jacobson RD, Valente KD, Barkovich AJ, Walsh CA. (2006) A familial syndrome of unilateral polymicrogyria affecting the right hemisphere. Neurology 66: 133–135.
- Clement E, Mercuri E, Godfrey C, Smith J, Robb S, Kinali M, Straub V, Bushby K, Manzur A, Talim B, Cowan F, Quinlivan R, Klein A, Longman C, Mcwilliam R, Topaloglu H, Mein R, Abbs S, North K, Barkovich AJ, Rutherford M, Muntoni F. (2008) Brain involvement in muscular dystrophies with defective dystroglycan glycosylation. Ann Neurol 64: 573–582.
- Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, Curry CJ, Mcdonald-Mcginn D, Medne L, Zackai EH, Parsons J, Zand DJ, Hisama FM, Walsh CA, Leventer RJ, Martin CL, Gajecka M, Shaffer LG. (2008) Consistent Chromosome Abnormalities Identify Novel Polymicrogyria Loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2. Am J Med Genet A 146A: 1637–1654.
- Evrard P, De Saint-Georges P, Kadhim HJ, Gadisseux J-F. (1989) Pathology of prenatal encephalopathies. In J French (Ed) Child neurology and developmental disabilities. Paul H. Brookes, Baltimore, pp. 153–176.
-
Friede RL. (1989) Developmental neuropathology, 2nd edn. Springer-Verlag, Berlin.
10.1007/978-3-642-73697-1 Google Scholar
- Guerrini R, Dravet C, Raybaud C, Roger J, Bureau M, Battaglia A, Livet MO, Gambarelli D, Robain O. (1992) Epilepsy and focal gyral anomalies detected by MRI: electroclinico-morphological correlations and follow-up. Dev Med Child Neurol 34: 706–718.
- Guerrini R, Dubeau F, Dulac O, Barkovich AJ, Kuzniecky R, Fett C, Jones-Gottman M, Canapicchi R, Cross H, Fish D, Bananni P, Jambaque I, Andermann F. (1997) Bilateral parasagittal parietooccipital polymicrogyria and epilepsy. Ann Neurol 41: 65–73.
- Guerrini R, Barkovich A, Sztriha L, Dobyns W. (2000) Bilateral frontal polymicrogyria. Neurology 54: 909–913.
- Hallervorden J. (1949) Ueber eine Kohlenoxydvergiftung im Fetalleben mit Entwicklunsstorung der Hirnrinde. Allg Z Psychiatr 124: 289–298.
- Haltia M, Leivo I, Somer H, Pihko H, Paetau A, Kivelä T, Tarkkanen A, Tomé F, Engvall E, Santavuori P. (1997) Muscle-eye-brain disease: a neuropathological study. Ann Neurol 41: 173–180.
- Jansen A, Andermann E. (2005) Genetics of the polymicrogyria syndromes. J Med Genet 42: 369–378.
- Kanagawa M, Toda T. (2006) The genetic and molecular basis of muscular dystrophy: roles of cell-matrix linkage in the pathogenesis. J Hum Genet 51: 915–926.
- Kuzniecky R, Andermann F, Guerrini R. (1993) Congenital bilateral perisylvian syndrome: study of 31 patients. The congenital bilateral perisylvian syndrome multicenter collaborative study. Lancet 341: 608–612.
- Kuzniecky R. (1994) Familial diffuse cortical dysplasia. Arch Neurol 51: 307–310.
- Leventer RJ, Lese CM, Cardosi C, Rosenberry J, Weiss A, Stoodley N. (2001) A study of 220 patients with polymicrogyria delineates distinct phenotypes and reveals genetic loci on chromosome 1p, 2p, 6q, 21q, 22q, and Xq. Am J Hum Genet 69: 177.
- Li S, Jin Z, Koirala S, Bu L, Xu L, Hynes RO, Walsh CA, Corfas G, Piao X. (2008) GPR56 Regulates Pial Basement Membrane Integrity and Cortical Lamination. J Neurosci 28: 5817–5826.
- Norman MG, Mcgillivray BC, Kalousek DK, Hill A, Poskitt KJ. (1995) Congenital malformations of the brain: pathologic, embryologic, clinical, radiologic and genetic aspects. Oxford University Press, Oxford.
- Piao X, Basel-Vanagaite L, Straussberg R, Grant P, Pugh E, Doheny K, Doan B, Hong S, Shugart Y, Walsh C. (2002) An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. Am J Hum Genet 70: 1028–1033.
- Roll P, Rudolf G, Pereira S, Royer B, Scheffer I, Massacrier A, Valenti M, Roeckel-Trevisiol N, Jamali S, Beclin C, Seegmuller C, Metz-Lutz M, Lemainque A, Delepine M, Caloustian C, De Saint Martin A, Bruneau N, Depétris D, Mattéi M, Flori E, Robaglia-Schlupp A, Lévy N, Neubauer B, Ravid R, Marescaux C, Berkovic S, Hirsch E, Lathrop M, Cau P, Szepetowski P. (2006) SRPX2 mutations in disorders of language cortex and cognition. Hum Mol Genet 15: 1195–1207.
- Takada K. (1988) Fukuyama congenital muscular dystrophy as a unique disorder of neuronal migration: a neuropathological review and hypothesis. Yonago Acta Med 31: 1–16.
- Takada K, Nakamura H, Takashima S. (1988) Cortical dysplasia in Fukuyama congenital muscular dystrophy: a Golgi and angioarchitectonic analysis. Acta Neuropathol 76: 170–178.
- Takanashi J, Barkovich A. (2003) The changing MR imaging appearance of polymicrogyria: a consequence of myelination. AJNR Am J Neuroradiol 24: 788–793.
- Van Reeuwijk J, Janssen M, Van Den Elzen C, Beltran-Valero De Bernabe D, Sabatelli P, Merlini L, Boon M, Scheffer H, Brockington M, Muntoni F, Huynen MA, Verrips A, Walsh CA, Barth PG, Brunner HG, Van Bokhoven H. (2005) POMT2 mutations cause {alpha}-dystroglycan hypoglycosylation and Walker-Warburg syndrome. J Med Genet 42: 907–912.
- Van Reeuwijk J, Grewal P, Salih M, Beltrán-Valero De Bernabé D, Mclaughlan J, Michielse C, Herrmann R, Hewitt J, Steinbrecher A, Seidahmed M, Shaheed M, Abomelha A, Brunner H, Van Bokhoven H, Voit T. (2007) Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome. Hum Genet 121: 685–690.
- Villard L, Nguyen K, Cardoso C, Martin C, Weiss A, Silfry-Platt M, Grix A, Graham J Jr, Winter R, Leventer R, Dobyns W. (2002) A locus for bilateral perisylvian polymicrogyria maps to Xq28. Am J Hum Genet 70: 1003–1008.
- Wright R, Johnson D, Neumann M, Ksiazek TG, Rollin P, Keech RV, Bonthius DJ, Hitchon P, Grose CF, Bell WE, Bale JF Jr. (1997) Congenital lymphocytic choriomeningitis virus syndrome: a disease that mimics congenital toxoplasmosis or Cytomegalovirus infection. Pediatrics 100: E9.