๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Determinants of parental decisions after the prenatal diagnosis of Down syndrome

โœ Scribed by Kramer, Ralph L.; Jarve, Robert K.; Yaron, Yuval; Johnson, Mark P.; Lampinen, Jenifer; Kasperski, Stefanie B.; Evans, Mark I.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
13 KB
Volume
79
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19980923)79:3<172::aid-ajmg4>3.0.co;2-p

No coin nor oath required. For personal study only.

โœฆ Synopsis


We evaluated demographic factors and factors specific to the current pregnancy, and their relationship to the decision to continue or terminate a pregnancy after prenatal diagnosis of Down syndrome. All cases of Down syndrome (DS) managed at a tertiary care center from 1989-1997 were retrospectively analyzed with respect to maternal age, parity, gestational age, sonographic findings, insurance status, and race. Of 145 cases of trisomy 21, 19 (13.1%) of women chose continuation of pregnancy, while 126 (86.9%) chose termination. There were no differences between groups in parity, sonographic findings, insurance status, or race at the time of diagnosis. However, patients who chose termination were significantly older and earlier in gestation than those electing to continue their pregnancy. When Down syndrome is diagnosed prenatally, the choice of termination is related to maternal age and gestational age, but only gestational age is a significant independent predictor of pregnancy termination.


๐Ÿ“œ SIMILAR VOLUMES


Prenatal diagnosis of the RSH/Smith-Leml
โœ Kratz, Lisa E.; Kelley, Richard I. ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 34 KB ๐Ÿ‘ 1 views

The RSH/Smith-Lemli-Opitz syndrome (RSH/SLOS) is a relatively common, autosomal recessive malformation syndrome comprising distinctive facial, limb and genital anomalies, and mental retardation. Most patients with a clinical diagnosis of RSH/SLOS have a defect of cholesterol biosynthesis at the leve

Prenatal diagnosis of Walker-Warburg syn
โœ Gasser, B.; Lindner, V.; Dreyfus, M.; Feidt, X.; Leissner, P.; Treisser, A.; Sto ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 41 KB ๐Ÿ‘ 1 views

Walker-Warburg syndrome (WWS) is an autosomal recessive condition characterized by diffuse neurodysplasia, resulting in brain and eye abnormalities. We report on 3 prenatally diagnosed cases of this syndrome born to a consanguineous couple. An ultrasonographic examination showed hydrocephalus at th

Parental decisions to terminate/continue
โœ Evans, Mark I.; Sobiecki, Michelle A.; Krivchenia, Eric L.; Duquette, Debra A.; ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 16 KB

This study was undertaken to determine if parental decisions to continue or terminate following the diagnosis of a cytogenetic abnormality have changed over the past 8 years at the same center. Parental decisions in 310 prenatal chromosomal abnormalities were stratified by procedure (chorionic vil-

Correlates of prenatal visceromegaly
โœ Barr, Mason ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 24 KB

Aside from recognized overgrowth syndromes, instances of visceromegaly are not uncommon at perinatal autopsy. The database of the University of Michigan Teratology Unit was screened for individual viscera exceeding the 90th centile for body and brain weight standards. The data were stratified for se

cover
โœ Josรฉ Manuel Aguilar ๐Ÿ“‚ Fiction ๐Ÿ“… 2013 ๐Ÿ› Almuzara ๐ŸŒ Spanish โš– 220 KB

Dirigido a padres y madres en proceso de separaciรณn o divorciados, psicรณlogos y trabajadores sociales, y a los profesionales que se encuentran implicados en los procesos de derecho de familia, como jueces, fiscales, abogados y forenses. La idea de que un progenitor manipule a sus hijos con intenciรณn

Prenatal diagnosis of a familial interch
โœ Ashton-Prolla, Patricia; Gershin, Irina F.; Babu, Arvind; Neu, Richard L.; Zinbe ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 10 KB ๐Ÿ‘ 1 views

An apparently unbalanced karyotype containing an abnormal chromosome 11 was identified in a 16-week female fetus by analysis of cultured amniocytes. Fluorescence in situ hybridization (FISH) with a chromosome 11 paint identified the presence of an insertion in band 11q24. Parental karyotyping docume