Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX

Journal de Gynecologie Obstetrique et Biologie de la Reproduction

Volumn 38, Issue 7, 2009, Pages 599-603

  Ben Hamouda, H ^a   Mkacher, N ^a   Elghezal, H ^b   Bannour, H ^a   Kamoun, M ^a   Soua, H ^a   Saad, A ^b   Souissi, M M ^a   Sfar, M T ^a  

^a Tahar Sfar University Hospital   (Tunisia)

^b FARHAT HACHED HOSPITAL   (Tunisia)

Author keywords

Prenatal diagnosis; Prognosis; Triple X syndrome

Indexed keywords

AMNIOCENTESIS; ARTICLE; BIRTH WEIGHT; CASE REPORT; CHILD; CLINICAL FEATURE; CONGENITAL MALFORMATION; DISEASE COURSE; EXTERNAL EAR MALFORMATION; FACE DYSMORPHIA; FEMALE; HUMAN; KARYOTYPE; KARYOTYPE 47,XXX; MALE; MATERNAL AGE; MICROPHTHALMIA; PHENOTYPE; PRENATAL DIAGNOSIS; PROGNOSIS;

CHILD; CHROMOSOMES, HUMAN, X; DEVELOPMENTAL DISABILITIES; FEMALE; HUMANS; KARYOTYPING; MATERNAL AGE; PREGNANCY; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS;

EID: 70350126944     PISSN: 03682315     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jgyn.2009.08.003     Document Type: Article

References (18)

1. Jacobs P.A., Baikie A.G., Court-Brown W.M., MacGregor T.N., Maclean N., and Harnden D.G. Evidence for the existence of the human. Lancet 2 (1959) 423-425
2. Simpson J.L., and Elias S. Sex chromosomal polysomies (47, XXY; 47, XYY; 47, XXX), sex reversed (46, XX) males, and disorders of the male reproductive ducts. In: Simpson J.L., and Elias S. (Eds). Genetics in obstetrics and gynecology (2003), Saunders, Philadelphia 323-341
3. Khoury-Cotlado F., Wehbeh A.N., Fisher A.J., Bombard A.T., and Weiner Z. Prenatal diagnosis of 47, XXX. Am J Obstet Gynecol 192 (2005) 1469-1471
4. Jagadeesh S., Jabeen G., Bhat L., Vasikarla M., Suresh A., Seshadri S., et al. Triple X syndrome with rare phenotypic presentation. Indian J Pediatr 75 (2008) 629-631
5. Kim E.S., and Gross T.L. Prenatal ultrasound detection of a congenital epulis in a triple X female fetus: a case report. Prenat Diagn 19 (1999) 774-776
6. Lin H.J., Ndiforchu F., and Patell S. Exstrophy of the cloaca in a 47, XXX child: review of genitourinary malformations in triple X patients. Am J Med Genet 45 (1993) 761-763
7. Rolle U., Linse B., Glasow S., Sandig K.R., Richter T., and Till H. Duodenal atresia in an infant with triple X syndrome: a new associated malformation in 47, triple X. Birth Defects Res A Clin Mol Teratol 79 (2007) 612-613
8. Haddow J.E., Palomaki G.E., Knight G.J., Cunningham G.C., Lustig L.S., and Boyd P.A. Reducing the need for amniocentesis in women 35 years of age or older with serum markers for screening. N Engl J Med 330 (1994) 1114-1118
9. Kellner L.H., Weiss R.R., Weiner Z., Neuer M., Martin G.M., Schulman H., et al. The advantages of using triple-marker screening for chromosomal abnormalities. Am J Obstet Gynecol 172 (1995) 831-836
10. Haddow J.E., Palomaki G.E., Knight G.J., Williams J., Pulkkinen A., Canick J.A., et al. Prenatal screening for Down's syndrome with the use of maternal serum marker. N Engl J Med 327 (1992) 588-593
11. Benn P.A., Horne D., Briganti S., and Greenstein R.M. Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome. Am J Obstet Gynecol 173 (1995) 496-501
12. Rembouskos G., Cicero S., Longo D., Sacchini C., and Nicolaides K.H. Single umbilical artery at 11-14 weeks' gestation: relation to chromosomal defects. Ultrasound Obstet Gynecol 22 (2003) 567-570
13. Krusinskie V., AIvesaIo L., and Sidlauskas A. The craniofacial complex in 47, XXX females. Eur J Orthod 27 (2005) 396-401
14. Perrotin F., Guichet A., Marret H., Potin J., Body G., and Lansac J. Devenir prénatal des anomalies des chromosomes sexuels diagnostiquées pendant la grossesse : analyse rétrospective de 47 cas. J Gynecol Obstet Biol Reprod 29 (2000) 668-676
15. Rosa R.F., Dibi R.P., Picetti Jdos S., Rosa R.C., Zen P.R., and Graziadio C. Amenorrhea and X chromosome abnormalities. Rev Bras Ginecol Obstet 30 (2008) 511-517
16. Goswami R., Goswami D., Kabra M., Gupta N., Dubey S., and Dadhwal V. Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders. Fertil Steril 80 (2003) 1052-1054
17. Kemp B., Hauptmann S., Schroder W., Amo-Takyi B., Leeners B., and Rath W. Dysgerminoma of the ovary in a patient with triple X syndrome. Int J Gynecol Obstet 50 (1995) 51-53
18. Lee J.H., Kim K.S., and Cho Y.G. A case of torsion of a mucinous cystadenoma in triple X syndrome with pure gonadal dysgenesis. Arch Gynecol Obstet 274 (2006) 174-177