Fetal Nörosonografide Kavum Septum Pellisidumun Önemi
References
Griffiths PD, Batty R, Reeves MJ, Connolly DJ. Imaging the corpus callosum, septum pellucidum and fornix in children: normal anatomy and variations of normality. Neuroradiology. 2009;51(5):337-45. doi: 10.1007/s00234-009-0506-y.
Rakic P, Yakovlev PI. Development of the corpus callosum and cavum septi in man. J Comp Neurol. 1968;132(1):45-72. doi: 10.1002/cne.901320103.
Callen PW, Callen AL, Glenn OA, Toi A. Columns of the fornix, not to be mistaken for the cavum septi pellucidi on prenatal sonography. J Ultrasound Med. 2008;27(1):25-31. doi: 10.7863/jum.2008.27.1.25.
Winter TC, Kennedy AM, Byrne J, Woodward PJ. The cavum septi pellucidi: why is it important? J Ultrasound Med. 2010;29(3):427-44. doi: 10.7863/jum.2010.29.3.427.
CSP, cavum septi pellucidi. SMFM. SMFM Anomalies Consult Series #3. Am J Obstet Gynecol. 2020. doi:https://doi.org/10.1016/j.ajog.2020.08.180
Barkovich AJ, Fram EK, Norman D. Septo-optic dysplasia: MR imaging. Radiology. 1989;171(1):189-92. doi: 10.1148/radiology.171.1.2928524.
Hosseinzadeh K, Luo J, Borhani A, Hill L. Non-visualisation of cavum septi pellucidi: implication in prenatal diagnosis? Insights Imaging. 2013;4(3):357-67. doi: 10.1007/s13244-013-0244-x.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A, Kuller JA, Craigo S, Fox NS, Norton ME, Post A, Rotmensch S, Ward A, Yeaton-Massey A. SMFM Fetal Anomalies Consult Series #3: Intracranial Anomalies. Am J Obstet Gynecol. 2020;223(6):B2-B50. doi: 10.1016/j.ajog.2020.08.041.
Fratelli N, Papageorghiou AT, Prefumo F, Bakalis S, Homfray T, Thilaganathan B. Outcome of prenatally diagnosed agenesis of the corpus callosum. Prenat Diagn. 2007;27(6):512-7. doi: 10.1002/pd.1719.
Oh KY, Kennedy AM, Frias AE Jr, Byrne JL. Fetal schizencephaly: pre- and postnatal imaging with a review of the clinical manifestations. Radiographics. 2005;25(3):647-57. doi: 10.1148/rg.253045103.
Howe DT, Rankin J, Draper ES. Schizencephaly prevalence, prenatal diagnosis and clues to etiology: a register-based study. Ultrasound Obstet Gynecol. 2012;39(1):75-82. doi: 10.1002/uog.9069.
Fogliarini C, Chaumoitre K, Chapon F, Fernandez C, Lévrier O, Figarella-Branger D, Girard N. Assessment of cortical maturation with prenatal MRI: part II: abnormalities of cortical maturation. Eur Radiol. 2005;15(9):1781-9. doi: 10.1007/s00330-005-2779-9.
Denis D, Chateil JF, Brun M, Brissaud O, Lacombe D, Fontan D, Flurin V, Pedespan J. Schizencephaly: clinical and imaging features in 30 infantile cases. Brain Dev. 2000;22(8):475-83. doi: 10.1016/s0387-7604(00)00173-x.
Orioli IM, Castilla EE. Epidemiology of holoprosencephaly: Prevalence and risk factors. Am J Med Genet C Semin Med Genet. 2010;154(1):13-21. doi: 10.1002/ajmg.c.30233.
Raman R, Mukunda Jagadesh G. Antenatal diagnosis of alobar holoprosencephaly. Case Rep Radiol. 2014;2014:724671. doi: 10.1155/2014/724671.
Naikwadi A, Rege R, Hameed S. Antenatal sonographic diagnosis of semilobar holoprosencephaly with associated cleft lip and palate. BJR Case Rep. 2018;5(1):20180013. doi: 10.1259/bjrcr.20180013.
Stashinko EE, Clegg NJ, Kammann HA, Sweet VT, Delgado MR, Hahn JS, Levey EB. A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly. Am J Med Genet A. 2004;128(2):114-9. doi: 10.1002/ajmg.a.30070.
Hahn JS, Barnes PD. Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation. Am J Med Genet C Semin Med Genet. 2010;154(1):120-32. doi: 10.1002/ajmg.c.30238.
Garne E, Loane M, Addor MC, Boyd PA, Barisic I, Dolk H. Congenital hydrocephalus--prevalence, prenatal diagnosis and outcome of pregnancy in four European regions. Eur J Paediatr Neurol. 2010;14(2):150-5. doi: 10.1016/j.ejpn.2009.03.005.
Prayer D, Brugger PC, Kasprian G, Witzani L, Helmer H, Dietrich W, Eppel W, Langer M. MRI of fetal acquired brain lesions. Eur J Radiol. 2006;57(2):233-49. doi: 10.1016/j.ejrad.2005.11.023.
Lam YH, Tang MH. Serial sonographic features of a fetus with hydranencephaly from 11 weeks to term. Ultrasound Obstet Gynecol. 2000;16(1):77-9. doi: 10.1046/j.1469-0705.2000.00165.x.
Rosette TH, Towbin RB, Schaefer CM, Towbin AJ, Aria DJ. Hydranencephaly. Appl Radiol. 2022;51(1):46-7.
Sepulveda W, Cortes-Yepes H, Wong AE, Dezerega V, Corral E, Malinger G. Prenatal sonography in hydranencephaly: findings during the early stages of disease. J Ultrasound Med. 2012;31(5):799-804. doi: 10.7863/jum.2012.31.5.799.
Traggiai C, Stanhope R. Endocrinopathies associated with midline cerebral and cranial malformations. J Pediatr 2002;140(2):252-5. doi: 10.1067/mpd.2002.121822.
Miller SP, Shevell MI, Patenaude Y, Poulin C, O'Gorman AM. Septo-optic dysplasia plus: a spectrum of malformations of cortical development. Neurology. 2000 25;54(8):1701-3. doi: 10.1212/wnl.54.8.1701.
Central nervous system: agenesis of the corpus callosum (ACC). in: Sanders R. Blackman L. Hogge W.A. Wulfsberg E.A. Speval P.J. Structural fetal abnormalities: the total picture. 2nd ed. CV Mosby Company, St Louis, MO2002: 17.
Vawter-Lee MM, Wasserman H, Thomas CW, Nichols B, Nagaraj UD, Schapiro M, Venkatesan C. Outcome of Isolated Absent Septum Pellucidum Diagnosed by Fetal Magnetic Resonance Imaging (MRI) Scan. J Child Neurol. 2018;33(11):693-9. doi: 10.1177/0883073818783460.
Rakic P, Yakovlev PI. Development of the corpus callosum and cavum septi in man. J Comp Neurol. 1968;132(1):45-72. doi: 10.1002/cne.901320103.
Callen PW, Callen AL, Glenn OA, Toi A. Columns of the fornix, not to be mistaken for the cavum septi pellucidi on prenatal sonography. J Ultrasound Med. 2008;27(1):25-31. doi: 10.7863/jum.2008.27.1.25.
Winter TC, Kennedy AM, Byrne J, Woodward PJ. The cavum septi pellucidi: why is it important? J Ultrasound Med. 2010;29(3):427-44. doi: 10.7863/jum.2010.29.3.427.
CSP, cavum septi pellucidi. SMFM. SMFM Anomalies Consult Series #3. Am J Obstet Gynecol. 2020. doi:https://doi.org/10.1016/j.ajog.2020.08.180
Barkovich AJ, Fram EK, Norman D. Septo-optic dysplasia: MR imaging. Radiology. 1989;171(1):189-92. doi: 10.1148/radiology.171.1.2928524.
Hosseinzadeh K, Luo J, Borhani A, Hill L. Non-visualisation of cavum septi pellucidi: implication in prenatal diagnosis? Insights Imaging. 2013;4(3):357-67. doi: 10.1007/s13244-013-0244-x.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A, Kuller JA, Craigo S, Fox NS, Norton ME, Post A, Rotmensch S, Ward A, Yeaton-Massey A. SMFM Fetal Anomalies Consult Series #3: Intracranial Anomalies. Am J Obstet Gynecol. 2020;223(6):B2-B50. doi: 10.1016/j.ajog.2020.08.041.
Fratelli N, Papageorghiou AT, Prefumo F, Bakalis S, Homfray T, Thilaganathan B. Outcome of prenatally diagnosed agenesis of the corpus callosum. Prenat Diagn. 2007;27(6):512-7. doi: 10.1002/pd.1719.
Oh KY, Kennedy AM, Frias AE Jr, Byrne JL. Fetal schizencephaly: pre- and postnatal imaging with a review of the clinical manifestations. Radiographics. 2005;25(3):647-57. doi: 10.1148/rg.253045103.
Howe DT, Rankin J, Draper ES. Schizencephaly prevalence, prenatal diagnosis and clues to etiology: a register-based study. Ultrasound Obstet Gynecol. 2012;39(1):75-82. doi: 10.1002/uog.9069.
Fogliarini C, Chaumoitre K, Chapon F, Fernandez C, Lévrier O, Figarella-Branger D, Girard N. Assessment of cortical maturation with prenatal MRI: part II: abnormalities of cortical maturation. Eur Radiol. 2005;15(9):1781-9. doi: 10.1007/s00330-005-2779-9.
Denis D, Chateil JF, Brun M, Brissaud O, Lacombe D, Fontan D, Flurin V, Pedespan J. Schizencephaly: clinical and imaging features in 30 infantile cases. Brain Dev. 2000;22(8):475-83. doi: 10.1016/s0387-7604(00)00173-x.
Orioli IM, Castilla EE. Epidemiology of holoprosencephaly: Prevalence and risk factors. Am J Med Genet C Semin Med Genet. 2010;154(1):13-21. doi: 10.1002/ajmg.c.30233.
Raman R, Mukunda Jagadesh G. Antenatal diagnosis of alobar holoprosencephaly. Case Rep Radiol. 2014;2014:724671. doi: 10.1155/2014/724671.
Naikwadi A, Rege R, Hameed S. Antenatal sonographic diagnosis of semilobar holoprosencephaly with associated cleft lip and palate. BJR Case Rep. 2018;5(1):20180013. doi: 10.1259/bjrcr.20180013.
Stashinko EE, Clegg NJ, Kammann HA, Sweet VT, Delgado MR, Hahn JS, Levey EB. A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly. Am J Med Genet A. 2004;128(2):114-9. doi: 10.1002/ajmg.a.30070.
Hahn JS, Barnes PD. Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation. Am J Med Genet C Semin Med Genet. 2010;154(1):120-32. doi: 10.1002/ajmg.c.30238.
Garne E, Loane M, Addor MC, Boyd PA, Barisic I, Dolk H. Congenital hydrocephalus--prevalence, prenatal diagnosis and outcome of pregnancy in four European regions. Eur J Paediatr Neurol. 2010;14(2):150-5. doi: 10.1016/j.ejpn.2009.03.005.
Prayer D, Brugger PC, Kasprian G, Witzani L, Helmer H, Dietrich W, Eppel W, Langer M. MRI of fetal acquired brain lesions. Eur J Radiol. 2006;57(2):233-49. doi: 10.1016/j.ejrad.2005.11.023.
Lam YH, Tang MH. Serial sonographic features of a fetus with hydranencephaly from 11 weeks to term. Ultrasound Obstet Gynecol. 2000;16(1):77-9. doi: 10.1046/j.1469-0705.2000.00165.x.
Rosette TH, Towbin RB, Schaefer CM, Towbin AJ, Aria DJ. Hydranencephaly. Appl Radiol. 2022;51(1):46-7.
Sepulveda W, Cortes-Yepes H, Wong AE, Dezerega V, Corral E, Malinger G. Prenatal sonography in hydranencephaly: findings during the early stages of disease. J Ultrasound Med. 2012;31(5):799-804. doi: 10.7863/jum.2012.31.5.799.
Traggiai C, Stanhope R. Endocrinopathies associated with midline cerebral and cranial malformations. J Pediatr 2002;140(2):252-5. doi: 10.1067/mpd.2002.121822.
Miller SP, Shevell MI, Patenaude Y, Poulin C, O'Gorman AM. Septo-optic dysplasia plus: a spectrum of malformations of cortical development. Neurology. 2000 25;54(8):1701-3. doi: 10.1212/wnl.54.8.1701.
Central nervous system: agenesis of the corpus callosum (ACC). in: Sanders R. Blackman L. Hogge W.A. Wulfsberg E.A. Speval P.J. Structural fetal abnormalities: the total picture. 2nd ed. CV Mosby Company, St Louis, MO2002: 17.
Vawter-Lee MM, Wasserman H, Thomas CW, Nichols B, Nagaraj UD, Schapiro M, Venkatesan C. Outcome of Isolated Absent Septum Pellucidum Diagnosed by Fetal Magnetic Resonance Imaging (MRI) Scan. J Child Neurol. 2018;33(11):693-9. doi: 10.1177/0883073818783460.
Pages
141-150
Published
April 3, 2023
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Kaya M. Fetal Nörosonografide Kavum Septum Pellisidumun Önemi. In: Kaya Ö, editor. Güncel Radyoloji Çalışmaları III [Internet]. Türkiye: Academician Publishing Book DOI Portal; 2023 [cited 2026 Jul. 16]. pp. 141-50. Available from: https://omp35.books.akademisyen.net/index.php/akya/catalog/book/2545/chapter/12711
