Fetal trisomy 13 distinguished by persistent fetal tachycardia

International Journal of Gynecology and Obstetrics

Volumn 57, Issue 3, 1997, Pages 317-318

  Shulman, L P ^a   Emerson, D S ^a   Phillips, O P ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

Fetal tachycardia; Maternal serum biochemical screening; Trisomy 13; Ultrasound

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHORION VILLUS SAMPLING; FEMALE; FETUS; FETUS ECHOGRAPHY; FETUS HEART RATE; FIRST TRIMESTER PREGNANCY; GENETIC COUNSELING; HUMAN; MATERNAL BLOOD; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TACHYCARDIA; TRISOMY 13;

EID: 0030941317     PISSN: 00207292     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0020-7292(97)02911-1     Document Type: Article

References (4)

1. Shulman LP, Emerson DS, Felker RE, Phillips OP, Simpson JL, Elias S. High frequency of cytogenetic abnormalities in fetuses with cystic hygroma diagnosed in the first trimester. Obstet Gynecol 1992; 80: 80-82.
2. Nicolaides KH, Brizot ML, Snijders RJM. Fetal nuchal translucency: ultrasound screening for fetal trisomy in the first trimester of pregnancy. Br J Obstet Gynaecol 1994; 101: 782-786.
3. Roberts LJ, Bewley S, Mackinson AM, Rodeck CH. First trimester fetal nuchal translucency: Problems with screening the general population 1. Br Obstet Gynaecol 1995; 102: 381-385.
4. Martinez JM, Comas C, Ojuel J, Borrell A, Puerto B, Fortuny A. Fetal heart rate patterns in pregnancies with chromosomal disorders or subsequent fetal loss. Obstet Gynecol 1996; 87: 118-121.