Diagnostic ultrasound ( PDFDrive )

1214 PART IV Obstetric and Fetal Sonography
170. Guibaud L, des Portes V. Plea for an anatomical approach to abnormalities
of the posterior fossa in prenatal diagnosis. Ultrasound Obstet Gynecol.
2006;27(5):477-481.
171. Robinson AJ, Blaser S, Toi A, et al. he fetal cerebellar vermis: assessment
for abnormal development by ultrasonography and magnetic resonance
imaging. Ultrasound Q. 2007;23(3):211-223.
172. Adamsbaum C, Moutard ML, Andre C, et al. MRI of the fetal posterior
fossa. Pediatr Radiol. 2005;35(2):124-140.
173. Patel S, Barkovich AJ. Analysis and classiication of cerebellar malformations.
AJNR Am J Neuroradiol. 2002;23(7):1074-1087.
174. Phillips JJ, Mahony BS, Siebert JR, et al. Dandy-Walker malformation
complex: correlation between ultrasonographic diagnosis and postmortem
neuropathology. Obstet Gynecol. 2006;107(3):685-693.
175. Parisi MA, Dobyns WB. Human malformations of the midbrain and
hindbrain: review and proposed classiication scheme. Mol Genet Metab.
2003;80(1-2):36-53.
176. Volpe P, Muto B, Passamonti U, et al. Abnormal sonographic appearance
of posterior brain at 11-14 weeks and fetal outcome. Prenat Diagn.
2015;35(7):717-723.
177. Chapman T, Mahalingam S, Ishak GE, et al. Diagnostic imaging of posterior
fossa anomalies in the fetus and neonate: part 2, Posterior fossa disorders.
Clin Imaging. 2015;39(2):167-175.
178. Babcook CJ, Chong BW, Salamat MS, et al. Sonographic anatomy of the
developing cerebellum: normal embryology can resemble pathology. AJR
Am J Roentgenol. 1996;166(2):427-433.
179. Pilu G, Hobbins JC. Sonography of fetal cerebrospinal anomalies. Prenat
Diagn. 2002;22(4):321-330.
180. Limperopoulos C, Robertson Jr RL, Khwaja OS, et al. How accurately does
current fetal imaging identify posterior fossa anomalies? AJR Am J Roentgenol.
2008;190(6):1637-1643.
181. Malinger G, Ginath S, Lerman-Sagie T, et al. he fetal cerebellar vermis:
normal development as shown by transvaginal ultrasound. Prenat Diagn.
2001;21(8):6876-6892.
182. Pasquier L, Marcorelles P, Loget P, et al. Rhombencephalosynapsis and
related anomalies: a neuropathological study of 40 fetal cases. Acta Neuropathol.
2009;117(2):185-200.
183. Poretti A, Leventer RJ, Cowan FM, et al. Cerebellar clet: a form of prenatal
cerebellar disruption. Neuropediatrics. 2008;39(2):106-112.
184. Boltshauser E, Martin F, Altermatt S. Outcome in children with spaceoccupying
posterior fossa arachnoid cysts. Neuropediatrics. 2002;33(3):
118-121.
185. Hayward R. Postnatal management and outcome for fetal-diagnosed intracerebral
cystic masses and tumours. Prenat Diagn. 2009;29(4):396-401.
186. de Wit MC, Lequin MH, de Coo IF, et al. Cortical brain malformations:
efect of clinical, neuroradiological, and modern genetic classiication. Arch
Neurol. 2008;65(3):358-366.
187. Montenegro MA, Guerreiro MM, Lopes-Cendes I, et al. Interrelationship
of genetics and prenatal injury in the genesis of malformations of cortical
development. Arch Neurol. 2002;59(7):1147-1153.
188. Toi A, Chitayat D, Blaser S. Abnormalities of the foetal cerebral cortex.
Prenat Diagn. 2009;29(4):355-371.
189. Wang DC, Shannon P, Toi A, et al. Temporal lobe dysplasia: a characteristic
sonographic inding in thanatophoric dysplasia. Ultrasound Obstet Gynecol.
2014;44(5):588-594.
190. Mirzaa GM, Paciorkowski AR. Introduction: brain malformations. Am J
Med Genet C Semin Med Genet. 2014;166C(2):117-123.
191. Raybaud C, Widjaja E. Development and dysgenesis of the cerebral cortex:
malformations of cortical development. Neuroimaging Clin N Am.
2011;21(3):483-543, vii.
192. Malinger G, Kidron D, Schreiber L, et al. Prenatal diagnosis of malformations
of cortical development by dedicated neurosonography. Ultrasound Obstet
Gynecol. 2007;29(2):178-191.
193. Malinger G, Lev D, Lerman-Sagie T. Assessment of fetal intracranial
pathologies irst demonstrated late in pregnancy: cell proliferation disorders.
Reprod Biol Endocrinol. 2003;1:110.
194. De Catte L, De Keersmaeker B, Claus F. Prenatal neurologic anomalies:
sonographic diagnosis and treatment. Paediatr Drugs. 2012;14(3):
143-155.
195. Guerrini R, Dobyns WB. Malformations of cortical development: clinical
features and genetic causes. Lancet Neurol. 2014;13(7):710-726.
196. Barkovich AJ, Kuzniecky RI, Jackson GD, et al. A developmental and genetic
classiication for malformations of cortical development. Neurology.
2005;65(12):1873-1887.
197. Soares de Olivera-Szejnfeld P, Levine D, Melo AS, et al. Congenital brain
abnormalities and Zika virus: what the radiologist can expect to see prenatally
and postnatally. Radiology. 2016;281(1):203-218.
198. Abuelo D. Microcephaly syndromes. Semin Pediatr Neurol. 2007;14(3):
118-127.
199. Schwarzler P, Homfray T, Bernard JP, et al. Late onset microcephaly: failure
of prenatal diagnosis. Ultrasound Obstet Gynecol. 2003;22(6):640-642.
200. Almgren M, Schalling M, Lavebratt C. Idiopathic megalencephaly—possible
cause and treatment opportunities: from patient to lab. Eur J Paediatr Neurol.
2008;12(6):438-445.
201. Malinger G, Lev D, Ben-Sira L, et al. Can syndromic macrocephaly be
diagnosed in utero? Ultrasound Obstet Gynecol. 2011;37(1):72-81.
202. Williams CA, Dagli A, Battaglia A. Genetic disorders associated with
macrocephaly. Am J Med Genet A. 2008;146A(15):2023-2037.
203. Olney AH. Macrocephaly syndromes. Semin Pediatr Neurol. 2007;14(3):
128-135.
204. Flores-Sarnat L. Hemimegalencephaly: part 1. Genetic, clinical, and imaging
aspects. J Child Neurol. 2002;17(5):373-384.
205. Andrade CS, Leite Cda C. Malformations of cortical development: current
concepts and advanced neuroimaging review. Arq Neuropsiquiatr.
2011;69(1):130-138.
206. Flores-Sarnat L. Hemimegalencephaly syndrome. Handb Clin Neurol.
2008;87:153-176.
207. Tinkle BT, Schorry EK, Franz DN, et al. Epidemiology of hemimegalencephaly:
a case series and review. Am J Med Genet A. 2005;139(3):
204-211.
208. Fry AE, Cushion TD, Pilz DT. he genetics of lissencephaly. Am J Med
Genet C Semin Med Genet. 2014;166C(2):198-210.
209. Lacalm A, Nadaud B, Massoud M, et al. Prenatal diagnosis of cobblestone
lissencephaly associated with Walker-Warburg syndrome based on a
speciic sonographic pattern. Ultrasound Obstet Gynecol. 2016;47(1):
117-122.
210. Stutterd CA, Leventer RJ. Polymicrogyria: a common and heterogeneous
malformation of cortical development. Am J Med Genet C Semin Med
Genet. 2014;166C(2):227-239.
211. Blondiaux E, Sileo C, Nahama-Allouche C, et al. Periventricular nodular
heterotopia on prenatal ultrasound and magnetic resonance imaging.
Ultrasound Obstet Gynecol. 2013;42(2):149-155.
212. Denis D, Chateil JF, Brun M, et al. Schizencephaly: clinical and imaging
features in 30 infantile cases. Brain Dev. 2000;22(8):475-483.
213. Denis D, Maugey-Laulom B, Carles D, et al. Prenatal diagnosis of schizencephaly
by fetal magnetic resonance imaging. Fetal Diagn her. 2001;16(6):
354-359.
214. Nissenkorn A, Michelson M, Ben-Zeev B, Lerman-Sagie T. Inborn errors
of metabolism: a cause of abnormal brain development. Neurology.
2001;56(10):1265-1272.
215. Spronsen FJ, Smit GP, Erwich JJ. Inherited metabolic diseases and pregnancy.
BJOG. 2005;112(1):2-11.
216. Strenge S, Froster UG, Wanders RJ, et al. First-trimester increased nuchal
translucency as a prenatal sign of Zellweger syndrome. Prenat Diagn.
2004;24(2):151-153.
217. Wortmann SB, Reimer A, Creemers JW, Mullaart RA. Prenatal diagnosis
of cerebral lesions in tuberous sclerosis complex (TSC). Case report and
review of the literature. Eur J Paediatr Neurol. 2008;12(2):123-126.
218. Northrup H, Koening M, Pearson D, Au K. Tuberous sclerosis complex.
GeneReviews. 2015. Available from: http://www.ncbi.nlm.nih.gov/books/
NBK1220/. Updated Sept. 3, 2015; accessed Feb. 13, 2016.
219. Levine D, Barnes P, Korf B, Edelman R. Tuberous sclerosis in the fetus:
second-trimester diagnosis of subependymal tubers with ultrafast MR
imaging. AJR Am J Roentgenol. 2000;175(4):1067-1069.
220. Santo S, D’Antonio F, Homfray T, et al. Counseling in fetal medicine:
agenesis of the corpus callosum. Ultrasound Obstet Gynecol. 2012;40(5):
513-521.