Urorectal septum malformation sequence: Ultrasound correlation with fetal examination

Indian Journal of Pediatrics

Volumn 73, Issue 4, 2006, Pages 287-293

  Patil, S J ^a   Phadke, Shubha R ^a  

^a SANJAY GANDHI POSTGRADUATE INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

Ambiguous genitalia; Anal atresia; Lower mesodermal defects; Urethral agenesis, hydronephrosis; Urorectal septum malformation sequence

Indexed keywords

ANORECTAL MALFORMATION; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; FETUS; FETUS MALFORMATION; GESTATIONAL AGE; HUMAN; KARYOTYPE; MALE; PERINATAL DEATH; REVIEW; UROGENITAL TRACT MALFORMATION; ANAL CANAL; ARTICLE; CASE REPORT; CONGENITAL MALFORMATION; ECHOGRAPHY; FATALITY; MULTIPLE MALFORMATION SYNDROME; OLIGOHYDRAMNIOS; PHYSICAL EXAMINATION; PREGNANCY; SYNDROME;

ABNORMALITIES, MULTIPLE; ANAL CANAL; FATAL OUTCOME; FEMALE; HUMANS; MALE; OLIGOHYDRAMNIOS; PHYSICAL EXAMINATION; PREGNANCY; SYNDROME; ULTRASONOGRAPHY, PRENATAL; UROGENITAL ABNORMALITIES;

EID: 33746895171     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02825821     Document Type: Review

References (12)

1. Escobar LF, Weaver DD, Bixler D, Hodes ME, Mitchell M. Urorectal septum malformation sequence: report of six cases and embryological analysis. Am J Dis Child 1987; 141 : 1021-1024.
2. Blott M, Nicoladies KH, Gibb D, Greenough A, Moscoso G, Campbell S. Fetal breathing movements as predictor of favorable pregnancy outcome after oligohydromnios due to membrane rupture in second trimester. Lancet 1987; 2 :129-131.
3. Sahinoglu Z, Mulayim B, Ozden S, Etker S, Celayir A, Ozkan F Biligic R. The prenatal diagnosis of cloacal dysgenesis sequence in six cases: can the termination of pregnancy always be the first choice?. Prenat Diagn 2004; 24 : 10-16.
4. Erickson RP, Stone JF, McNoe LA, Eccles MR. Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies. Clin Genet 1997; 51 : 331-337.
5. Wheeler PG, Weaver DD. Partial urorectal septum malformation sequence: A report of 25 cases. Am J Med Genet 2001; 103 : 99-105.
6. Pauli MR. Lower mesodermal defects: A common cause of fetal and early neonatal death. Am J Med Genet 1994; 50 : 154-172.
7. Wheeler PG, Weaver DD, Obeime MO, Vance GH, Bull MJ, Escobar LF. Urorectal septum malformation sequence: report of thirteen additional cases and review of the literature. Am J Med Genet 1997; 73 : 456-462.
8. Seaver LH, Grimes J, Erickson RP. Female pseudohermaphroditism with multiple caudal anomalies: Absence of Y-specific DNA sequences as pathogenetic factors. Am J Med Genet 1994; 51 : 16-21.
9. Martinez-Frias ML, Bermejo E, Garcia A, Galan E, Prieto L. Holoprosencephaly associated with caudal dysgenesis: A clinical-epidemiological analysis. Am J Med Genet 1994; 53 : 46-51.
10. Wei X, Sulik KK. Pathogenesis of caudal dysgenesis/sirenomelia induced by Ochratoxin A in chick embryos. Teratology 1996; 53 : 378-391.
11. Alles AJ, Sulik KK. A review of caudal dysgenesis and its pathogenesis as illustrated in an animal model. Birth defects Orig Artic Ser 1993; 29(1) : 83-102.
12. Mills PL, Pergament E. Urorectal septal defects in a female and her offspring. Am J Med Genet 1997; 70 : 250-252.