A FALSE-POSITIVE DIAGNOSIS OF TURNER SYNDROME BY AMNIOCENTESIS
โ Scribed by M. J. GRIFFITHS; P. R. MILLER; H. M. STIBBE
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 316 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0197-3851
No coin nor oath required. For personal study only.
โฆ Synopsis
A 45,X karyotype was observed in all cells examined from an amniotic 0uid sample taken at 16 weeks' gestation from a 37-year-old patient referred because of her age. Following termination of the pregnancy, all cells examined from fetal tissues (cardiac blood, skin, and muscle) showed a 46,XX karyotype. The most likely explanation for the discordant results is thought to be a dizygotic twin pregnancy with a normal fetus and an empty sac, the latter being sampled at amniocentesis resulting in a 45,X karyotype.
๐ SIMILAR VOLUMES
Maternal age-speciยฎc rates of Down syndrome used in serum screening
## Abstract ## Objective In routine practice, diagnosis of knee osteoarthritis (OA) currently relies on the combination of conventional risk factors and the presence of cardinal signs and symptoms. However, their role in early diagnosis has received little attention compared with biomarker researc
The aims of this systematic literature review are to estimate termination rates after prenatal diagnosis of one of five conditions: Down syndrome, spina bifida, anencephaly, and Turner and Klinefelter syndromes, and to determine the extent to which rates vary across conditions and with year of publi