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Different polymicrogyria patterns and associated anomalies in childhood: MRI findings

Yıl 2019, Cilt: 41 Sayı: 3, 531 - 536, 30.09.2019

Nisa Başpınar , Mehmet Atalar Bülent Yıldız İsmail Şalk

https://doi.org/10.7197/223.vi.613523

Öz

Polymicrogyria
is a developmental anomaly which has been diagnosed in recent years due to
improvements in neuroimaging methods. It may present with very different
clinical findings. It can be seen in many different patterns. It can be found
with different nervous system anomalies. In this article, different
polymicrogyria patterns and associated anomalies detected in childhood are
presented with MRI findings.

Anahtar Kelimeler

Magnetic resonance imaging Polymicrogyria Cerebrum

Kaynakça

  • 1. Leventer RJ, Guerrini R, Dobyns WB. Malformations of cortical development and epilepsy. Dialogues. Clin Neurosci. 2008; 10: 47-62.
  • 2. Golden JA, Harding BN. Cortical malformations: unfolding polymicrogyria. Nat Rev Neurol. 2010; 6: 471-72.
  • 3. Barkovich AJ, Gressens P, Evrard P. Formation, maturation, and disorders of brain neocortex. AJNR Am J Neuroradiol 1992; 13: 423–46.
  • 4. Evrard P, de Saint-Georges P, Kadhim HJ, Gadisseux JF. Pathology of prenatal encephalopathies. In: French J (ed) Child neurology and developmental disabilities. Paul H. Brookes, Baltimore, 1989, pp 153–76
  • 5. Englund C, Fink A, Lau C et al. Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex. J Neurosci 2005; 25: 247–51
  • 6. Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, et al. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and21q2. Am J Med Genet A 2008; 146: 1637–54
  • 7. Robin NH, Taylor CJ, Donald-McGinn DM, Zackai EH, Bingham P,Collins KJ, et al. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet. 2006; 140: 2416–25.
  • 8. Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. Classification system for malformations of cortical development: update 2001. Neurology 2001; 57: 2168–78.
  • 9. Öztoprak B, Atalar MH. Aberrant fissure in polymicrogyria. Cumhuriyet Medical Journal. 2016; 3: 185-194.
  • 10. Jansen AC, Robtaille Y, Honavar M, Mullatti N, Leventer RJ, Andermann E, Andermann F, Squier W. The histopathology of polymicrogyria: a series of 71 brain autopsy studies. Dev Med Child Neurol 2016; 58: 39-48.
  • 11. Hayashi N, Tsutsumi Y, Barkovich AJ. Morphological features and associated anomalies of schizencephaly in the clinical population: detailed analysis of MR images. Neuroradiology 2002; 44: 418–27.
  • 12. Guerrini R, Dravet C, Raybaud C et al. Epilepsy and focalgyral anomalies detected by MRI: electroclinico-morphological correlations and follow-up. Dev Med Child Neurol 1992; 34: 706–18.
  • 13. Takanashi J, Barkovich AJ. The changing MR imaging apearance of Polimicrogyria: A consequence of myelination. AJNR Am J Neuroradiology 2003; 4: 788-93

Yıl 2019, Cilt: 41 Sayı: 3, 531 - 536, 30.09.2019

Nisa Başpınar , Mehmet Atalar Bülent Yıldız İsmail Şalk

https://doi.org/10.7197/223.vi.613523

Öz

Kaynakça

  • 1. Leventer RJ, Guerrini R, Dobyns WB. Malformations of cortical development and epilepsy. Dialogues. Clin Neurosci. 2008; 10: 47-62.
  • 2. Golden JA, Harding BN. Cortical malformations: unfolding polymicrogyria. Nat Rev Neurol. 2010; 6: 471-72.
  • 3. Barkovich AJ, Gressens P, Evrard P. Formation, maturation, and disorders of brain neocortex. AJNR Am J Neuroradiol 1992; 13: 423–46.
  • 4. Evrard P, de Saint-Georges P, Kadhim HJ, Gadisseux JF. Pathology of prenatal encephalopathies. In: French J (ed) Child neurology and developmental disabilities. Paul H. Brookes, Baltimore, 1989, pp 153–76
  • 5. Englund C, Fink A, Lau C et al. Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex. J Neurosci 2005; 25: 247–51
  • 6. Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, et al. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and21q2. Am J Med Genet A 2008; 146: 1637–54
  • 7. Robin NH, Taylor CJ, Donald-McGinn DM, Zackai EH, Bingham P,Collins KJ, et al. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet. 2006; 140: 2416–25.
  • 8. Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. Classification system for malformations of cortical development: update 2001. Neurology 2001; 57: 2168–78.
  • 9. Öztoprak B, Atalar MH. Aberrant fissure in polymicrogyria. Cumhuriyet Medical Journal. 2016; 3: 185-194.
  • 10. Jansen AC, Robtaille Y, Honavar M, Mullatti N, Leventer RJ, Andermann E, Andermann F, Squier W. The histopathology of polymicrogyria: a series of 71 brain autopsy studies. Dev Med Child Neurol 2016; 58: 39-48.
  • 11. Hayashi N, Tsutsumi Y, Barkovich AJ. Morphological features and associated anomalies of schizencephaly in the clinical population: detailed analysis of MR images. Neuroradiology 2002; 44: 418–27.
  • 12. Guerrini R, Dravet C, Raybaud C et al. Epilepsy and focalgyral anomalies detected by MRI: electroclinico-morphological correlations and follow-up. Dev Med Child Neurol 1992; 34: 706–18.
  • 13. Takanashi J, Barkovich AJ. The changing MR imaging apearance of Polimicrogyria: A consequence of myelination. AJNR Am J Neuroradiology 2003; 4: 788-93
Toplam 13 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Sağlık Kurumları Yönetimi
Bölüm Medical Science Research Makaleler
Yazarlar

Nisa Başpınar

Mehmet Atalar

Bülent Yıldız

İsmail Şalk

Yayımlanma Tarihi 30 Eylül 2019
Kabul Tarihi 2 Eylül 2019
Yayımlandığı Sayı Yıl 2019 Cilt: 41 Sayı: 3

Kaynak Göster

AMA Başpınar N, Atalar M, Yıldız B, Şalk İ. Different polymicrogyria patterns and associated anomalies in childhood: MRI findings. CMJ. Eylül 2019;41(3):531-536. doi:10.7197/223.vi.613523