메뉴 건너뛰기




Volumn 26, Issue 2, 2006, Pages 389-405

Prenatal US and MR imaging findings of lissencephaly: Review of fetal cerebral sulcal development

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN CORTEX; BRAIN DISEASE; CONGENITAL MALFORMATION; ECHOGRAPHY; HUMAN; IMAGE ENHANCEMENT; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PRENATAL DEVELOPMENT; REVIEW;

EID: 33645555215     PISSN: 15271323     EISSN: 15271323     Source Type: Journal    
DOI: 10.1148/rg.262055059     Document Type: Review
Times cited : (105)

References (38)
  • 1
    • 0023946887 scopus 로고
    • Classification of congenital abnormalities of the CNS
    • van der Knaap MS, Valk J. Classification of congenital abnormalities of the CNS. AJNR Am J Neuroradiol 1988;9:315-326.
    • (1988) AJNR Am J Neuroradiol , vol.9 , pp. 315-326
    • Van Der Knaap, M.S.1    Valk, J.2
  • 4
    • 0002089308 scopus 로고
    • The development of the central nervous system during intrauterinc life
    • Falkner F, ed. Philadelphia, Pa: Saunders
    • Larroche J. The development of the central nervous system during intrauterinc life. In: Falkner F, ed. Human development. Philadelphia, Pa: Saunders, 1966; 257-260.
    • (1966) Human Development , pp. 257-260
    • Larroche, J.1
  • 5
    • 0035139527 scopus 로고    scopus 로고
    • Fetal cerebral cortex: Normal gestational landmarks identified using prenatal MR imaging
    • Garel C, Chantrel E, Brisse H, et al. Fetal cerebral cortex: normal gestational landmarks identified using prenatal MR imaging. AJNR Am J Neuroradiol 2001;22:184-189.
    • (2001) AJNR Am J Neuroradiol , vol.22 , pp. 184-189
    • Garel, C.1    Chantrel, E.2    Brisse, H.3
  • 7
    • 0030966443 scopus 로고    scopus 로고
    • Development of fetal gyri, sulci and fissures: A transvaginal sonographic study
    • Monteagudo A, Timor-Tritsch IE. Development of fetal gyri, sulci and fissures: a transvaginal sonographic study. Ultrasound Obstet Gynecol 1997;9: 222-228.
    • (1997) Ultrasound Obstet Gynecol , vol.9 , pp. 222-228
    • Monteagudo, A.1    Timor-Tritsch, I.E.2
  • 8
    • 10644279999 scopus 로고    scopus 로고
    • How early are fetal cerebral sulci visible at prenatal ultrasound and what is the normal pattern of early fetal sulcal development?
    • Toi A, Lister WS, Fong KW. How early are fetal cerebral sulci visible at prenatal ultrasound and what is the normal pattern of early fetal sulcal development? Ultrasound Obstet Gynecol 2004;24: 706-715.
    • (2004) Ultrasound Obstet Gynecol , vol.24 , pp. 706-715
    • Toi, A.1    Lister, W.S.2    Fong, K.W.3
  • 9
    • 0032976438 scopus 로고    scopus 로고
    • Cortical maturation in normal and abnormal fetuses as assessed with prenatal MR imaging
    • Levine D, Barnes P. Cortical maturation in normal and abnormal fetuses as assessed with prenatal MR imaging. Radiology 1999;210:751-758.
    • (1999) Radiology , vol.210 , pp. 751-758
    • Levine, D.1    Barnes, P.2
  • 10
    • 0033595252 scopus 로고    scopus 로고
    • Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly
    • Dobyns WB, Truwit CL, Ross ME, et al. Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly. Neurology 1999;53:270-277.
    • (1999) Neurology , vol.53 , pp. 270-277
    • Dobyns, W.B.1    Truwit, C.L.2    Ross, M.E.3
  • 11
    • 0031044984 scopus 로고    scopus 로고
    • Muscle-eye-brain disease: A neuropathological study
    • Haltia M, Leivo I, Somer H, et al. Muscle-eye-brain disease: a neuropathological study. Ann Neurol 1997;41:173-180.
    • (1997) Ann Neurol , vol.41 , pp. 173-180
    • Haltia, M.1    Leivo, I.2    Somer, H.3
  • 12
    • 0025824525 scopus 로고
    • Cerebro-ocular dysplasia-muscular dystrophy (Walker Warburg) syndrome: Findings in 20-week-old fetus
    • Miller G, Ladda RL, Towfighi J. Cerebro-ocular dysplasia-muscular dystrophy (Walker Warburg) syndrome: findings in 20-week-old fetus. Acta Neuropathol (Berlin) 1991;82:234-238.
    • (1991) Acta Neuropathol (Berlin) , vol.82 , pp. 234-238
    • Miller, G.1    Ladda, R.L.2    Towfighi, J.3
  • 13
    • 0027180939 scopus 로고
    • Development of the cortical dysplasia of type II lissencephaly
    • Squier MV. Development of the cortical dysplasia of type II lissencephaly. Neuropathol Appl Neurobiol 1993;19:209-213.
    • (1993) Neuropathol Appl Neurobiol , vol.19 , pp. 209-213
    • Squier, M.V.1
  • 14
    • 0024539092 scopus 로고
    • Diagnostic criteria for Walker-Warburg syndrome
    • Dobyns WB, Pagon RA, Armstrong D, et al. Diagnostic criteria for Walker-Warburg syndrome. Am J Med Genet 1989; 32:195-210.
    • (1989) Am J Med Genet , vol.32 , pp. 195-210
    • Dobyns, W.B.1    Pagon, R.A.2    Armstrong, D.3
  • 18
    • 10644295602 scopus 로고    scopus 로고
    • Prenatal ultrasound findings of lissencephaly associated with Miller-Dieker syndrome and comparison with pre- And postnatal magnetic resonance imaging
    • Fong KW, Ghai S, Toi A, Blaser S, Winsor EJ, Chitayat D. Prenatal ultrasound findings of lissencephaly associated with Miller-Dieker syndrome and comparison with pre- and postnatal magnetic resonance imaging. Ultrasound Obstet Gynecol 2004;24:716-723.
    • (2004) Ultrasound Obstet Gynecol , vol.24 , pp. 716-723
    • Fong, K.W.1    Ghai, S.2    Toi, A.3    Blaser, S.4    Winsor, E.J.5    Chitayat, D.6
  • 19
    • 33645581717 scopus 로고    scopus 로고
    • Miller-Dicker syndrome
    • Benacerraf BR, ed. Philadelphia, Pa: Churchill Livingstone
    • Benacerraf BR. Miller-Dicker syndrome. In: Benacerraf BR, ed. Ultrasound of fetal syndromes. Philadelphia, Pa: Churchill Livingstone, 1998; 130-132.
    • (1998) Ultrasound of Fetal Syndromes , pp. 130-132
    • Benacerraf, B.R.1
  • 20
    • 0030884066 scopus 로고    scopus 로고
    • Second-trimester diagnosis of fetal cataract in a fetus with Walker-Warburg syndrome
    • Beinder EJ, Pfeiffer RA, Bornemann A, Wenkel H. Second-trimester diagnosis of fetal cataract in a fetus with Walker-Warburg syndrome. Fetal Diagn Ther 1997; 12:197-199.
    • (1997) Fetal Diagn Ther , vol.12 , pp. 197-199
    • Beinder, E.J.1    Pfeiffer, R.A.2    Bornemann, A.3    Wenkel, H.4
  • 21
    • 0029877170 scopus 로고    scopus 로고
    • First-trimester sonographic detection of neurodevelopmental abnormalities in some singlegene disorders
    • van Zalen-Sprock RM, van Vugt JM, van Geijn HP. First-trimester sonographic detection of neurodevelopmental abnormalities in some singlegene disorders. Prenat Diagn 1996;16:199-202.
    • (1996) Prenat Diagn , vol.16 , pp. 199-202
    • Van Zalen-Sprock, R.M.1    Van Vugt, J.M.2    Van Geijn, H.P.3
  • 22
    • 0035093764 scopus 로고    scopus 로고
    • WalkerWarburg syndrome: Case report and review of the literature
    • Monteagudo A, Alayon A, Mayberry P. WalkerWarburg syndrome: case report and review of the literature. J Ultrasound Med 2001;20:419-426.
    • (2001) J Ultrasound Med , vol.20 , pp. 419-426
    • Monteagudo, A.1    Alayon, A.2    Mayberry, P.3
  • 23
    • 0005652032 scopus 로고    scopus 로고
    • Walker-Warburg syndrome
    • Benacerraf BR, ed. Philadelphia, Pa: Churchill Livingstone
    • Benacerraf BR. Walker-Warburg syndrome. In: Benacerraf BR, ed. Ultrasound of fetal syndromes. Philadelphia, Pa: Churchill Livingstone, 1998; 134-137.
    • (1998) Ultrasound of Fetal Syndromes , pp. 134-137
    • Benacerraf, B.R.1
  • 24
    • 0031794931 scopus 로고    scopus 로고
    • Antenatal diagnosis of isolated lissencephaly by ultrasound and magnetic resonance imaging
    • Greco P, Resta M, Vimercati A, et al. Antenatal diagnosis of isolated lissencephaly by ultrasound and magnetic resonance imaging. Ultrasound Obstet Gynecol 1998;12:276-279.
    • (1998) Ultrasound Obstet Gynecol , vol.12 , pp. 276-279
    • Greco, P.1    Resta, M.2    Vimercati, A.3
  • 26
    • 33645567896 scopus 로고    scopus 로고
    • Congenital muscular dystrophy
    • Blaser S, ed. Salt Lake City, Utah: Amirsys
    • Blaser S. Congenital muscular dystrophy. In: Blaser S, ed. Pocket radiologist: PedsNeuro, top 100 diagnoses. Salt Lake City, Utah: Amirsys, 2003; 57-59.
    • (2003) Pocket Radiologist: PedsNeuro, Top 100 Diagnoses , pp. 57-59
    • Blaser, S.1
  • 27
    • 0027314631 scopus 로고
    • Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome
    • Kimura S, Sasaki Y, Kobayashi T, et al. Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome. Brain Dev 1993;15: 182-191.
    • (1993) Brain Dev , vol.15 , pp. 182-191
    • Kimura, S.1    Sasaki, Y.2    Kobayashi, T.3
  • 28
    • 0036156420 scopus 로고    scopus 로고
    • Prenatal diagnosis of lissencephaly (type II) by ultrasound and fast magnetic resonance imaging
    • Kojima K, Suzuki Y, Seki K, et al. Prenatal diagnosis of lissencephaly (type II) by ultrasound and fast magnetic resonance imaging. Fetal Diagn Ther 2002;17:34-36.
    • (2002) Fetal Diagn Ther , vol.17 , pp. 34-36
    • Kojima, K.1    Suzuki, Y.2    Seki, K.3
  • 29
    • 0037390829 scopus 로고    scopus 로고
    • Lissencephaly and the molecular basis of neuronal migration
    • Kato M, Dobyns WB. Lissencephaly and the molecular basis of neuronal migration. Hum Mol Genet 2003;12:R89-R96.
    • (2003) Hum Mol Genet , vol.12
    • Kato, M.1    Dobyns, W.B.2
  • 30
    • 0038757833 scopus 로고    scopus 로고
    • 14-3-3ε is important for neuronal migration by binding to NUDFL: A molecular explanation for Miller-Dieker syndrome
    • Toyo-oka K, Shionoya A, Gambello MJ, et al. 14-3-3ε is important for neuronal migration by binding to NUDFL: a molecular explanation for Miller-Dieker syndrome. Nat Genet 2003;34: 274-285
    • (2003) Nat Genet , vol.34 , pp. 274-285
    • Toyo-Oka, K.1    Shionoya, A.2    Gambello, M.J.3
  • 31
    • 0037385481 scopus 로고    scopus 로고
    • Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3
    • Cardoso C, Leventer RJ, Ward HL, et al. Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3. Am J Hum Genet 2003;72:918-930.
    • (2003) Am J Hum Genet , vol.72 , pp. 918-930
    • Cardoso, C.1    Leventer, R.J.2    Ward, H.L.3
  • 33
    • 7844223263 scopus 로고    scopus 로고
    • LIS 1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
    • Pilz DT, Matsumoto N, Minnerath S, et al. LIS 1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum Mol Genet 1998;7:2029-2037.
    • (1998) Hum Mol Genet , vol.7 , pp. 2029-2037
    • Pilz, D.T.1    Matsumoto, N.2    Minnerath, S.3
  • 34
    • 17444444915 scopus 로고    scopus 로고
    • A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
    • des Portes V, Pinard JM, Billuart P, et al. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 1998;92:51-61.
    • (1998) Cell , vol.92 , pp. 51-61
    • Des Portes, V.1    Pinard, J.M.2    Billuart, P.3
  • 35
    • 0038185363 scopus 로고    scopus 로고
    • Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome
    • Beltran-Valero de Bernabe D, Currier S, Steinbrecher A, et al. Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. Am J Hum Genet 2002.;71:1033-1043.
    • (2002) Am J Hum Genet , vol.71 , pp. 1033-1043
    • Beltran-Valero De Bernabe, D.1    Currier, S.2    Steinbrecher, A.3
  • 36
    • 18044400450 scopus 로고    scopus 로고
    • Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase
    • Yoshida A, Kobayashi K, Manya H, et al. Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1. Dev Cell 2001;1:717-724.
    • (2001) POMGnT1. Dev Cell , vol.1 , pp. 717-724
    • Yoshida, A.1    Kobayashi, K.2    Manya, H.3
  • 37
    • 0032560851 scopus 로고    scopus 로고
    • An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
    • Kobayashi K, Nakahori Y, Miyake M, et al. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 1998;394:388-392.
    • (1998) Nature , vol.394 , pp. 388-392
    • Kobayashi, K.1    Nakahori, Y.2    Miyake, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.