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Taiwanese Journal of Obstetrics and Gynecology
Volume 46, Issue 3
, Pages 199-208
, September 2007
Prenatal Diagnosis of Iniencephaly
References
-
Saint-Hilaire IG. Iniencephalus. In: Bailliere JB, ed. Histoire des Anomalies de l'Organisation, Vol 2. Paris, 1836;308-10.
- . Prenatal diagnosis and pathoanatomy of iniencephaly . Clin Genet . 1986;30:81–86
-
.
Iniencephalus
.
Can Med Assoc J
. 1948;59:474–475
-
.
A report of two cases of iniencephalus
.
J Obstet Gynaecol Br Emp
. 1951;58:462–464
-
.
Iniencephalus
.
Am J Obstet
. 1897;35:11–53
-
.
Iniencephalus
.
J Obstet Gynaecol Br Emp
. 1939;46:25–31
-
.
Iniencephaly
.
In:
Woodward PJ
, Kennedy A
, Sohaey R
, Byrne JLB
, Oh KY
, Puchalski MD
editor.
Diagnostic Imaging: Obstetrics
. Salt Lake City: Amirsys Inc; 2005;p. 10–14
- . Antenatal ultrasound diagnosis of iniencephaly . J Clin Ultrasound . 1987;15:550–554
- . Prenatal ultrasonic diagnosis of a rare case of iniencephaly apertus . J Clin Ultrasound . 1987;15:200–203
- . Iniencephaly: prenatal ultrasonographic diagnosis—a case report . J Perinat Med . 1988;16:139–143
- . Iniencephaly: prenatal and postnatal findings . Geburtshilfe Frauenheilkd . 1990;50:491–494 [In German]
- . Iniencephaly: a case report . J Reprod Med . 1992;37:885–888
- . Endovaginal sonographic diagnosis of iniencephaly apertus and craniorachischisis at 13 weeks, menstrual age . J Clin Ultrasound . 1993;21:124–127
- . Endovaginal sonographic diagnosis of craniorachischisis at 13 weeks of gestation . Fetal Diagn Ther . 1994;9:391–394
- . Iniencephaly: sonographic-pathologic correlation of 19 cases . J Perinat Med . 1996;24:501–511
- . Trisomy 18 with total craniorachischisis and thoraco-abdominoschisis . Prenat Diagn . 1999;19:580–582
- . Iniencephaly: prenatal diagnosis and management . Prenat Diagn . 2000;20:202–205
- . Prenatal diagnosis in three cases of iniencephaly with unusual postmortem findings . Prenat Diagn . 2001;21:558–562
- . Sirenomelia sequence associated with craniorachischisis totalis, limb reduction and primitive heart . Indian Pediatr . 2001;38:1041–1045
- . Diagnosis of an unusual form of iniencephaly in the first trimester of pregnancy . Ultrasound Obstet Gynecol . 2001;18:549–551
- . Iniencephaly: four cases and a review of the literature . J Gynecol Obstet Biol Reprod (Paris) . 2002;31:276–282 [In French]
- . Iniencephaly and early prenatal diagnosis . J Gynecol Obstet Biol Reprod (Paris) . 2002;31:387–389 [In French]
- . Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report . Prenat Diagn . 2002;22:1240–1241
- . Transvaginal sonographic diagnosis of iniencephaly apertus and craniorachischisis at 9 weeks' gestation . Ultrasound Obstet Gynecol . 2003;22:657–658
- . Prenatal ultrasonographic diagnosis of iniencephaly . J Obstet Gynaecol . 2003;23:572–573
- . Iniencephaly and chromosome mosaicism: a report of two cases . Congenit Anom (Kyoto) . 2005;45:102–105
- . Prenatal diagnosis of pentalogy of Cantrell in three cases, two with craniorachischisis . J Clin Ultrasound . 2005;33:308–311
- . Neural tube defects and omphalocele in trisomy 18 . Clin Genet . 1988;34:98–103
- . Neural tube defects and omphalocele in trisomy 18 . Clin Genet . 1989;35:77–78
- . Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus) . J Med Genet . 1974;11:69–75
- . Malformations of the central nervous system in trisomy 18 syndrome . J Pediatr . 1966;69:771–778
- . Neural tube defects in trisomy 18 . Prenat Diagn . 1986;6:97–99
- . Neural tube defects, chromosome aberrations and multiple closure sites for the human neural tube . Clin Dysmorphol . 1995;4:202–207
- Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 . Nature . 1996;381:238–241
- Characterization of the human jumonji gene . Hum Mol Genet . 1996;5:1637–1641
- . The Klippel-Feil syndrome: genetic and clinical reevaluation of cervical fusion . Medicine (Baltimore) . 1967;46:491–512
- . Familial Klippel-Feil syndrome and paracentric inversion inv(8) (q22.2q23.3) . Am J Hum Genet . 1995;57:1364–1370
- . De novo apparently balanced reciprocal translocation between 5q11.2 and 17q23 associated with Klippel-Feil anomaly and type A1 brachydactyly . Am J Med Genet . 1995;57:447–449
- . De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia . Eur J Pediatr . 2003;162:594–597
- . Familial Klippel-Feil anomaly and t(5;8)(q35.1;p21.1) translocation . Am J Med Genet A . 2006;140:1013–1015
PII: S1028-4559(08)60021-2
doi: 10.1016/S1028-4559(08)60021-2
© 2007 Taiwan Association of Obstetric & Gynecology. Published by Elsevier Inc. All rights reserved.
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Taiwanese Journal of Obstetrics and Gynecology
Volume 46, Issue 3
, Pages 199-208
, September 2007
