Prenatal diagnosis of double trisomy 48,XXX,+18 in the first trimester

Journal of Ultrasound in Medicine

Volumn 24, Issue 5, 2005, Pages 717-719

  Dezerega, Victor ^a   Be, Cecilia ^b   Wong, Amy E ^a   Silva, Rafael ^a   Sepulveda, Waldo ^a,b  

^a Fetal Medicine Interest Group GIMEF   (Chile)

^b CLÍNICA LAS CONDES   (Chile)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANAMNESIS; ARTICLE; CASE REPORT; DOWN SYNDROME; FEMALE; FETUS ECHOGRAPHY; FETUS MONITORING; FIRST TRIMESTER PREGNANCY; HUMAN; KARYOTYPE; METAPHASE CHROMOSOME; PRENATAL DIAGNOSIS; PRENATAL SCREENING; TRISOMY; TRISOMY 48; X CHROMOSOME;

EID: 17744364295     PISSN: 02784297     EISSN: None     Source Type: Journal    
DOI: 10.7863/jum.2005.24.5.717     Document Type: Article

References (8)

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2. Chen CP, Chern SR, Yeh LF, Chen WL, Chen LF, Wang W. Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18. Prenat Diagn 2000; 20:750-753.
3. Snijders RJ, Noble P, Sebire N, Souka A, Nicolaides KH. UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks' gestation. Lancet 1998; 352:343-346.
4. Nicolaides KH, Sebire NJ, Snijders RJM. The 11-14 Week Scan: The Diagnosis of Fetal Abnormalities. Carnforth, England: Parthenon Publishing; 1999.
5. Nicolaides KH. Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities. Am J Obstet Gynecol 2004; 191:45-67.
6. van Huizen ME, Knegt AC, Bijlsma EK, Bilardo CM. Double trisomy 48,XXX,+18 in association with increased nuchal translucency: two cases. Prenat Diagn 2004; 24:1020-1021.
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8. Sebire NJ, Snijders RJ, Brown R, Southall T, Nicolaides KH. Detection of sex chromosome abnormalities by nuchal translucency screening at 10-14 weeks. Prenat Diagn 1998; 18:581-584.